Canonical Allele Identifier: CA344544922

Gene: CR1

Linked Data

• gnomAD v4: 1-207611680-G-T
• MyVariant Identifiers: chr1:g.207785025G>T (hg19) ; chr1:g.207611680G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611680G>T , CM000663.2:g.207611680G>T	GRCh38
NC_000001.10:g.207785025G>T , CM000663.1:g.207785025G>T	GRCh37
NC_000001.9:g.205851648G>T	NCBI36
NG_007481.1:g.120553G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6299G>T MANE Select	ENSP00000356016.4:p.Cys2100Phe
ENST00000367051.6:c.4949G>T	ENSP00000356018.1:p.Cys1650Phe
ENST00000367052.6:c.4949G>T	ENSP00000356019.1:p.Cys1650Phe
ENST00000367053.6:c.4949G>T	ENSP00000356020.1:p.Cys1650Phe
ENST00000400960.7:c.4949G>T	ENSP00000383744.2:p.Cys1650Phe
ENST00000367049.8:c.6299G>T	ENSP00000356016.4:p.Cys2100Phe
ENST00000367051.5:c.4949G>T	ENSP00000356018.1:p.Cys1650Phe
ENST00000367052.5:c.4949G>T	ENSP00000356019.1:p.Cys1650Phe
ENST00000367053.5:c.4949G>T	ENSP00000356020.1:p.Cys1650Phe
ENST00000400960.6:c.4949G>T	ENSP00000383744.2:p.Cys1650Phe
ENST00000529814.1:c.1180-4895G>T
NM_000573.3:c.4949G>T	NP_000564.2:p.Cys1650Phe
NM_000651.4:c.6299G>T	NP_000642.3:p.Cys2100Phe
XM_006711166.2:c.6314G>T	XP_006711229.1:p.Cys2105Phe
XM_011509205.1:c.6314G>T	XP_011507507.1:p.Cys2105Phe
NM_000651.5:c.6299G>T	NP_000642.3:p.Cys2100Phe
XM_024453287.1:c.4964G>T	XP_024309055.1:p.Cys1655Phe
NM_000573.4:c.4949G>T	NP_000564.2:p.Cys1650Phe
NM_000651.6:c.6299G>T MANE Select	NP_000642.3:p.Cys2100Phe