Human (GRCh38.p14)
Description

complement C1r [Source:HGNC Symbol;Acc:HGNC:1246]

Location

Chromosome 12: 7,080,214-7,092,540 reverse strand.

GRCh38:CM000674.2

View alleles of this gene on alternative sequences

About this gene

This gene has 16 transcripts (splice variants), 1 gene allele, 165 orthologues, 16 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000647956.2C1R-2142488705aaENSP00000497341.1
 
Protein coding
CCDS81658A0A3B3ISR2 NM_001733.7MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000536053.6C1R-2022347719aaENSP00000444271.3
 
Protein coding
CCDS86272B4DPQ0 -GENCODE basicTSL:2
ENST00000535233.6C1R-2012211671aaENSP00000438636.3
 
Protein coding
F5H2D0 -GENCODE basicTSL:2
ENST00000649804.1C1R-2161107351aaENSP00000497938.1
 
Protein coding
A0A3B3ITU4 -CDS 5' incomplete
ENST00000541042.5C1R-20859171aaENSP00000441601.1
 
Protein coding
F5GWL0 -TSL:5CDS 3' incomplete
ENST00000540242.2C1R-205575156aaENSP00000442946.1
 
Protein coding
F5H6Y3 -TSL:4CDS 3' incomplete
ENST00000538050.5C1R-20455349aaENSP00000444009.1
 
Protein coding
F5H1N6 -TSL:4CDS 3' incomplete
ENST00000543835.5C1R-210521156aaENSP00000445285.1
 
Protein coding
F5H3N3 -TSL:4CDS 3' incomplete
ENST00000540610.5C1R-20751993aaENSP00000439223.1
 
Protein coding
F5H3A3 -TSL:4CDS 3' incomplete
ENST00000543362.5C1R-209832144aaENSP00000446356.1
 
Nonsense mediated decay
F5H1V0 -TSL:3
ENST00000648162.1C1R-2151881No protein-
 
Protein coding CDS not defined
---
ENST00000540394.5C1R-2063501No protein-
 
Retained intron
--TSL:2
ENST00000602298.2C1R-2132580No protein-
 
Retained intron
--TSL:2
ENST00000536092.1C1R-203632No protein-
 
Retained intron
--TSL:1
ENST00000545466.1C1R-212597No protein-
 
Retained intron
--TSL:2
ENST00000543851.1C1R-211476No protein-
 
Retained intron
--TSL:4