Canonical Allele Identifier: CA1139849128

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207472977G= , CM000663.2:g.207472977G=	GRCh38
NC_000001.10:g.207646322G= , CM000663.1:g.207646322G=	GRCh37
NC_000001.9:g.205712945G=	NCBI36
NG_013006.1:g.23678G= , LRG_348:g.23678G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.1407G=	ENSP00000514480.1:p.Leu469=
ENST00000699621.1:c.1396G=
ENST00000367057.8:c.1776G= MANE Select	ENSP00000356024.3:p.Leu592=
ENST00000367057.7:c.1776G=	ENSP00000356024.3:p.Leu592=
ENST00000367058.7:c.1776G=	ENSP00000356025.3:p.Leu592=
ENST00000367059.3:c.1776G=	ENSP00000356026.3:p.Leu592=
NM_001006658.2:c.1776G= , LRG_348t1:c.1776G=	NP_001006659.1:p.Leu592=
NM_001877.4:c.1776G=	NP_001868.2:p.Leu592=
XM_011509206.1:c.1407G=	XP_011507508.1:p.Leu469=
XM_011509206.3:c.1407G=	XP_011507508.1:p.Leu469=
NM_001006658.3:c.1776G= MANE Select	NP_001006659.1:p.Leu592=
NM_001877.5:c.1776G=	NP_001868.2:p.Leu592=