Canonical Allele Identifier: CA344545233

Gene: CR1

Linked Data

• MyVariant Identifiers: chr1:g.207785169A>T (hg19) ; chr1:g.207611824A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611824A>T , CM000663.2:g.207611824A>T	GRCh38
NC_000001.10:g.207785169A>T , CM000663.1:g.207785169A>T	GRCh37
NC_000001.9:g.205851792A>T	NCBI36
NG_007481.1:g.120697A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6443A>T MANE Select	ENSP00000356016.4:p.Asp2148Val
ENST00000367051.6:c.5093A>T	ENSP00000356018.1:p.Asp1698Val
ENST00000367052.6:c.5093A>T	ENSP00000356019.1:p.Asp1698Val
ENST00000367053.6:c.5093A>T	ENSP00000356020.1:p.Asp1698Val
ENST00000400960.7:c.5093A>T	ENSP00000383744.2:p.Asp1698Val
ENST00000367049.8:c.6443A>T	ENSP00000356016.4:p.Asp2148Val
ENST00000367051.5:c.5093A>T	ENSP00000356018.1:p.Asp1698Val
ENST00000367052.5:c.5093A>T	ENSP00000356019.1:p.Asp1698Val
ENST00000367053.5:c.5093A>T	ENSP00000356020.1:p.Asp1698Val
ENST00000400960.6:c.5093A>T	ENSP00000383744.2:p.Asp1698Val
ENST00000529814.1:c.1180-4751A>T
NM_000573.3:c.5093A>T	NP_000564.2:p.Asp1698Val
NM_000651.4:c.6443A>T	NP_000642.3:p.Asp2148Val
XM_006711166.2:c.6458A>T	XP_006711229.1:p.Asp2153Val
XM_011509205.1:c.6458A>T	XP_011507507.1:p.Asp2153Val
NM_000651.5:c.6443A>T	NP_000642.3:p.Asp2148Val
XM_024453287.1:c.5108A>T	XP_024309055.1:p.Asp1703Val
NM_000573.4:c.5093A>T	NP_000564.2:p.Asp1698Val
NM_000651.6:c.6443A>T MANE Select	NP_000642.3:p.Asp2148Val