Canonical Allele Identifier: CA1143950609

Gene: CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207611813G= , CM000663.2:g.207611813G=	GRCh38
NC_000001.10:g.207785158G= , CM000663.1:g.207785158G=	GRCh37
NC_000001.9:g.205851781G=	NCBI36
NG_007481.1:g.120686G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.6432G= MANE Select	ENSP00000356016.4:p.Thr2144=
ENST00000367051.6:c.5082G=	ENSP00000356018.1:p.Thr1694=
ENST00000367052.6:c.5082G=	ENSP00000356019.1:p.Thr1694=
ENST00000367053.6:c.5082G=	ENSP00000356020.1:p.Thr1694=
ENST00000400960.7:c.5082G=	ENSP00000383744.2:p.Thr1694=
ENST00000367049.8:c.6432G=	ENSP00000356016.4:p.Thr2144=
ENST00000367051.5:c.5082G=	ENSP00000356018.1:p.Thr1694=
ENST00000367052.5:c.5082G=	ENSP00000356019.1:p.Thr1694=
ENST00000367053.5:c.5082G=	ENSP00000356020.1:p.Thr1694=
ENST00000400960.6:c.5082G=	ENSP00000383744.2:p.Thr1694=
ENST00000529814.1:c.1180-4762G=
NM_000573.3:c.5082G=	NP_000564.2:p.Thr1694=
NM_000651.4:c.6432G=	NP_000642.3:p.Thr2144=
XM_006711166.2:c.6447G=	XP_006711229.1:p.Thr2149=
XM_011509205.1:c.6447G=	XP_011507507.1:p.Thr2149=
NM_000651.5:c.6432G=	NP_000642.3:p.Thr2144=
XM_024453287.1:c.5097G=	XP_024309055.1:p.Thr1699=
NM_000573.4:c.5082G=	NP_000564.2:p.Thr1694=
NM_000651.6:c.6432G= MANE Select	NP_000642.3:p.Thr2144=