Canonical Allele Identifier: CA344545092

Gene: CR1

Linked Data

• COSMIC: COSM4135940 ; COSM4135941
• MyVariant Identifiers: chr1:g.207785103T>A (hg19) ; chr1:g.207611758T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611758T>A , CM000663.2:g.207611758T>A	GRCh38
NC_000001.10:g.207785103T>A , CM000663.1:g.207785103T>A	GRCh37
NC_000001.9:g.205851726T>A	NCBI36
NG_007481.1:g.120631T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6377T>A MANE Select	ENSP00000356016.4:p.Phe2126Tyr
ENST00000367051.6:c.5027T>A	ENSP00000356018.1:p.Phe1676Tyr
ENST00000367052.6:c.5027T>A	ENSP00000356019.1:p.Phe1676Tyr
ENST00000367053.6:c.5027T>A	ENSP00000356020.1:p.Phe1676Tyr
ENST00000400960.7:c.5027T>A	ENSP00000383744.2:p.Phe1676Tyr
ENST00000367049.8:c.6377T>A	ENSP00000356016.4:p.Phe2126Tyr
ENST00000367051.5:c.5027T>A	ENSP00000356018.1:p.Phe1676Tyr
ENST00000367052.5:c.5027T>A	ENSP00000356019.1:p.Phe1676Tyr
ENST00000367053.5:c.5027T>A	ENSP00000356020.1:p.Phe1676Tyr
ENST00000400960.6:c.5027T>A	ENSP00000383744.2:p.Phe1676Tyr
ENST00000529814.1:c.1180-4817T>A
NM_000573.3:c.5027T>A	NP_000564.2:p.Phe1676Tyr
NM_000651.4:c.6377T>A	NP_000642.3:p.Phe2126Tyr
XM_006711166.2:c.6392T>A	XP_006711229.1:p.Phe2131Tyr
XM_011509205.1:c.6392T>A	XP_011507507.1:p.Phe2131Tyr
NM_000651.5:c.6377T>A	NP_000642.3:p.Phe2126Tyr
XM_024453287.1:c.5042T>A	XP_024309055.1:p.Phe1681Tyr
NM_000573.4:c.5027T>A	NP_000564.2:p.Phe1676Tyr
NM_000651.6:c.6377T>A MANE Select	NP_000642.3:p.Phe2126Tyr