Canonical Allele Identifier: CA1139926082

Gene: CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207580276A= , CM000663.2:g.207580276A=	GRCh38
NC_000001.10:g.207753621A= , CM000663.1:g.207753621A=	GRCh37
NC_000001.9:g.205820244A=	NCBI36
NG_007481.1:g.89149A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.4973A= MANE Select	ENSP00000356016.4:p.His1658=
ENST00000367051.6:c.3623A=	ENSP00000356018.1:p.His1208=
ENST00000367052.6:c.3623A=	ENSP00000356019.1:p.His1208=
ENST00000367053.6:c.3623A=	ENSP00000356020.1:p.His1208=
ENST00000400960.7:c.3623A=	ENSP00000383744.2:p.His1208=
ENST00000367049.8:c.4973A=	ENSP00000356016.4:p.His1658=
ENST00000367051.5:c.3623A=	ENSP00000356018.1:p.His1208=
ENST00000367052.5:c.3623A=	ENSP00000356019.1:p.His1208=
ENST00000367053.5:c.3623A=	ENSP00000356020.1:p.His1208=
ENST00000400960.6:c.3623A=	ENSP00000383744.2:p.His1208=
ENST00000529814.1:c.1179+14353A=
ENST00000534202.5:c.*738A=	ENSP00000436139.2:n.*738A=
NM_000573.3:c.3623A=	NP_000564.2:p.His1208=
NM_000651.4:c.4973A=	NP_000642.3:p.His1658=
XM_006711166.2:c.4988A=	XP_006711229.1:p.His1663=
XM_011509205.1:c.4988A=	XP_011507507.1:p.His1663=
NM_000651.5:c.4973A=	NP_000642.3:p.His1658=
XM_024453287.1:c.3638A=	XP_024309055.1:p.His1213=
NM_000573.4:c.3623A=	NP_000564.2:p.His1208=
NM_000651.6:c.4973A= MANE Select	NP_000642.3:p.His1658=