Canonical Allele Identifier: CA383729603

Gene: C1R C1RL

Linked Data

• MyVariant Identifiers: chr12:g.7244101A>C (hg19) ; chr12:g.7091505A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.7091505A>C , CM000674.2:g.7091505A>C	GRCh38
NC_000012.11:g.7244101A>C , CM000674.1:g.7244101A>C	GRCh37
NC_000012.10:g.7135242A>C	NCBI36
NG_062465.1:g.6103T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647956.2:c.178T>G (C1R) MANE Select	ENSP00000497341.1:p.Phe60Val
ENST00000535233.6:c.178T>G (C1R)	ENSP00000438636.3:p.Phe60Val
ENST00000536053.6:c.220T>G (C1R)	ENSP00000444271.3:p.Phe74Val
ENST00000536092.1:n.283T>G (C1R)
ENST00000538050.5:c.-138T>G (C1R)	ENSP00000444009.1:n.-138T>G
ENST00000539803.5:c.645T>G (C1RL)
ENST00000540242.2:c.178T>G (C1R)	ENSP00000442946.1:p.Phe60Val
ENST00000540394.5:n.937T>G (C1R)
ENST00000540610.5:c.-85+882T>G (C1R)	ENSP00000439223.1:n.-85+882T>G
ENST00000541042.5:c.-138T>G (C1R)	ENSP00000441601.1:n.-138T>G
ENST00000542285.5:c.178T>G (C1R)	ENSP00000438615.2:p.Phe60Val
ENST00000543362.5:c.178T>G (C1R)	ENSP00000446356.1:p.Phe60Val
ENST00000543835.5:c.178T>G (C1R)	ENSP00000445285.1:p.Phe60Val
ENST00000545466.1:n.231T>G (C1R)
NM_001733.4:c.178T>G (C1R)	NP_001724.3:p.Phe60Val
NM_001354346.1:c.220T>G (C1R)	NP_001341275.1:p.Phe74Val
NM_001733.6:c.178T>G (C1R)	NP_001724.4:p.Phe60Val
NM_001733.7:c.178T>G (C1R) MANE Select	NP_001724.4:p.Phe60Val
NM_001354346.2:c.220T>G (C1R)	NP_001341275.1:p.Phe74Val