Canonical Allele Identifier: CA1140016534

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207473553T= , CM000663.2:g.207473553T=	GRCh38
NC_000001.10:g.207646898T= , CM000663.1:g.207646898T=	GRCh37
NC_000001.9:g.205713521T=	NCBI36
NG_013006.1:g.24254T= , LRG_348:g.24254T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001006658.3:c.1987T= MANE Select	NP_001006659.1:p.Ser663=
ENST00000367057.8:c.1987T= MANE Select	ENSP00000356024.3:p.Ser663=
NM_001006658.2:c.1987T= , LRG_348t1:c.1987T=	NP_001006659.1:p.Ser663=
NM_001877.4:c.1979-248T=	NP_001868.2:n.1979-248T=
NM_001877.5:c.1979-248T=	NP_001868.2:n.1979-248T=
ENST00000367057.7:c.1987T=	ENSP00000356024.3:p.Ser663=
ENST00000367058.7:c.1979-248T=	ENSP00000356025.3:n.1979-248T=
ENST00000367059.3:c.1979-248T=	ENSP00000356026.3:n.1979-248T=
ENST00000699620.1:c.1610-248T=	ENSP00000514480.1:n.1610-248T=
ENST00000699621.1:c.1599-248T=
XM_011509206.1:c.1618T=	XP_011507508.1:p.Ser540=
XM_011509206.3:c.1618T=	XP_011507508.1:p.Ser540=