Canonical Allele Identifier: CA10912759

Gene: CR1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207630250G>A , CM000663.2:g.207630250G>A	GRCh38
NC_000001.10:g.207803595G>A , CM000663.1:g.207803595G>A	GRCh37
NC_000001.9:g.205870218G>A	NCBI36
NG_007481.1:g.139123G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.7353-267G>A MANE Select	ENSP00000356016.4:n.7353-267G>A
ENST00000367051.6:c.6003-267G>A	ENSP00000356018.1:n.6003-267G>A
ENST00000367052.6:c.6003-267G>A	ENSP00000356019.1:n.6003-267G>A
ENST00000367053.6:c.6003-267G>A	ENSP00000356020.1:n.6003-267G>A
ENST00000400960.7:c.6003-267G>A	ENSP00000383744.2:n.6003-267G>A
ENST00000367049.8:c.7353-267G>A	ENSP00000356016.4:n.7353-267G>A
ENST00000367051.5:c.6003-267G>A	ENSP00000356018.1:n.6003-267G>A
ENST00000367052.5:c.6003-267G>A	ENSP00000356019.1:n.6003-267G>A
ENST00000367053.5:c.6003-267G>A	ENSP00000356020.1:n.6003-267G>A
ENST00000400960.6:c.6003-267G>A	ENSP00000383744.2:n.6003-267G>A
ENST00000529814.1:c.1871-267G>A
NM_000573.3:c.6003-267G>A	NP_000564.2:n.6003-267G>A
NM_000651.4:c.7353-267G>A	NP_000642.3:n.7353-267G>A
XM_006711166.2:c.7367+7182G>A	XP_006711229.1:n.7367+7182G>A
XM_011509205.1:c.7368-267G>A	XP_011507507.1:n.7368-267G>A
NM_000651.5:c.7353-267G>A	NP_000642.3:n.7353-267G>A
XM_024453287.1:c.6018-267G>A	XP_024309055.1:n.6018-267G>A
NM_000573.4:c.6003-267G>A	NP_000564.2:n.6003-267G>A
NM_000651.6:c.7353-267G>A MANE Select	NP_000642.3:n.7353-267G>A