Canonical Allele Identifier: CA2483411841

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207472884A= , CM000663.2:g.207472884A=	GRCh38
NC_000001.10:g.207646229A= , CM000663.1:g.207646229A=	GRCh37
NC_000001.9:g.205712852A=	NCBI36
NG_013006.1:g.23585A= , LRG_348:g.23585A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000699620.1:c.1314A=	ENSP00000514480.1:p.Glu438=
ENST00000699621.1:c.1303A=
ENST00000367057.8:c.1683A= MANE Select	ENSP00000356024.3:p.Glu561=
ENST00000640301.1:c.133A=	ENSP00000491608.1:n.133A=
ENST00000367057.7:c.1683A=	ENSP00000356024.3:p.Glu561=
ENST00000367058.7:c.1683A=	ENSP00000356025.3:p.Glu561=
ENST00000367059.3:c.1683A=	ENSP00000356026.3:p.Glu561=
NM_001006658.2:c.1683A= , LRG_348t1:c.1683A=	NP_001006659.1:p.Glu561=
NM_001877.4:c.1683A=	NP_001868.2:p.Glu561=
XM_011509206.1:c.1314A=	XP_011507508.1:p.Glu438=
XM_011509206.3:c.1314A=	XP_011507508.1:p.Glu438=
NM_001006658.3:c.1683A= MANE Select	NP_001006659.1:p.Glu561=
NM_001877.5:c.1683A=	NP_001868.2:p.Glu561=