Canonical Allele Identifier: CA2483433209

Gene: CR1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207523745G= , CM000663.2:g.207523745G=	GRCh38
NC_000001.10:g.207697090G= , CM000663.1:g.207697090G=	GRCh37
NC_000001.9:g.205763713G=	NCBI36
NG_007481.1:g.32618G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367049.9:c.622G= MANE Select	ENSP00000356016.4:p.Val208=
ENST00000367051.6:c.487+12091G=	ENSP00000356018.1:n.487+12091G=
ENST00000367052.6:c.622G=	ENSP00000356019.1:p.Val208=
ENST00000367053.6:c.622G=	ENSP00000356020.1:p.Val208=
ENST00000400960.7:c.622G=	ENSP00000383744.2:p.Val208=
ENST00000367049.8:c.622G=	ENSP00000356016.4:p.Val208=
ENST00000367050.8:n.743G=
ENST00000367051.5:c.487+12091G=	ENSP00000356018.1:n.487+12091G=
ENST00000367052.5:c.622G=	ENSP00000356019.1:p.Val208=
ENST00000367053.5:c.622G=	ENSP00000356020.1:p.Val208=
ENST00000400960.6:c.622G=	ENSP00000383744.2:p.Val208=
ENST00000434033.5:n.549G=
ENST00000436595.1:n.414+12091G=
ENST00000450439.5:n.549G=
ENST00000529814.1:c.549G=
ENST00000534202.5:c.622G=	ENSP00000436139.2:p.Val208=
NM_000573.3:c.622G=	NP_000564.2:p.Val208=
NM_000651.4:c.622G=	NP_000642.3:p.Val208=
XM_006711166.2:c.637G=	XP_006711229.1:p.Val213=
XM_011509205.1:c.637G=	XP_011507507.1:p.Val213=
NM_000651.5:c.622G=	NP_000642.3:p.Val208=
XM_024453287.1:c.637G=	XP_024309055.1:p.Val213=
NM_000573.4:c.622G=	NP_000564.2:p.Val208=
NM_000651.6:c.622G= MANE Select	NP_000642.3:p.Val208=