Human (GRCh38.p14)
Description

angiotensinogen [Source:HGNC Symbol;Acc:HGNC:333]

Gene Synonyms

SERPINA8

About this transcript

This transcript has 5 exons, is annotated with 37 domains and features, is associated with 19258 variant alleles and maps to 366 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000366667.6AGT-2012116476aaENSP00000355627.5
 
Protein coding
CCDS1585P01019 NM_001384479.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000680783.1AGT-2095004285aaENSP00000506329.1
 
Protein coding
A0A7P0TAP4 -GENCODE basic
ENST00000680041.1AGT-2082632476aaENSP00000504866.1
 
Protein coding
CCDS1585A0A7P0T8D1 P01019 -GENCODE basicAPPRIS P1
ENST00000681514.1AGT-2122571476aaENSP00000505963.1
 
Protein coding
CCDS1585A0A7P0T8D1 P01019 -GENCODE basicAPPRIS P1
ENST00000681269.1AGT-2102141476aaENSP00000505985.1
 
Protein coding
CCDS1585A0A7P0T8D1 P01019 -GENCODE basicAPPRIS P1
ENST00000679957.1AGT-2071933473aaENSP00000506646.1
 
Protein coding
A0A7P0TBH1 -GENCODE basic
ENST00000679684.1AGT-2031915420aaENSP00000505981.1
 
Protein coding
A0A7P0TA52 -GENCODE basic
ENST00000681772.1AGT-2135410366aaENSP00000505829.1
 
Nonsense mediated decay
A0A7P0T9S6 --
ENST00000679802.1AGT-2055135286aaENSP00000505184.1
 
Nonsense mediated decay
A0A7P0Z441 --
ENST00000679738.1AGT-2044894476aaENSP00000505063.1
 
Nonsense mediated decay
CCDS1585A0A7P0T8D1 P01019 --
ENST00000679854.1AGT-2068609No protein-
 
Retained intron
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ENST00000681347.1AGT-2116410No protein-
 
Retained intron
---
ENST00000657140.1AGT-2022114No protein-
 
Retained intron
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Statistics

Exons: 5, Coding exons: 4, Transcript length: 2,141 bps, Translation length: 476 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: P01019

CCDS

This transcript is a member of the Human CCDS set: CCDS1585

Version

ENST00000681269.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.