Canonical Allele Identifier: CA344545089

Gene: CR1

Linked Data

• MyVariant Identifiers: chr1:g.207785102T>G (hg19) ; chr1:g.207611757T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611757T>G , CM000663.2:g.207611757T>G	GRCh38
NC_000001.10:g.207785102T>G , CM000663.1:g.207785102T>G	GRCh37
NC_000001.9:g.205851725T>G	NCBI36
NG_007481.1:g.120630T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6376T>G MANE Select	ENSP00000356016.4:p.Phe2126Val
ENST00000367051.6:c.5026T>G	ENSP00000356018.1:p.Phe1676Val
ENST00000367052.6:c.5026T>G	ENSP00000356019.1:p.Phe1676Val
ENST00000367053.6:c.5026T>G	ENSP00000356020.1:p.Phe1676Val
ENST00000400960.7:c.5026T>G	ENSP00000383744.2:p.Phe1676Val
ENST00000367049.8:c.6376T>G	ENSP00000356016.4:p.Phe2126Val
ENST00000367051.5:c.5026T>G	ENSP00000356018.1:p.Phe1676Val
ENST00000367052.5:c.5026T>G	ENSP00000356019.1:p.Phe1676Val
ENST00000367053.5:c.5026T>G	ENSP00000356020.1:p.Phe1676Val
ENST00000400960.6:c.5026T>G	ENSP00000383744.2:p.Phe1676Val
ENST00000529814.1:c.1180-4818T>G
NM_000573.3:c.5026T>G	NP_000564.2:p.Phe1676Val
NM_000651.4:c.6376T>G	NP_000642.3:p.Phe2126Val
XM_006711166.2:c.6391T>G	XP_006711229.1:p.Phe2131Val
XM_011509205.1:c.6391T>G	XP_011507507.1:p.Phe2131Val
NM_000651.5:c.6376T>G	NP_000642.3:p.Phe2126Val
XM_024453287.1:c.5041T>G	XP_024309055.1:p.Phe1681Val
NM_000573.4:c.5026T>G	NP_000564.2:p.Phe1676Val
NM_000651.6:c.6376T>G MANE Select	NP_000642.3:p.Phe2126Val