Canonical Allele Identifier: CA1369005

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207475071G>A , CM000663.2:g.207475071G>A	GRCh38
NC_000001.10:g.207648416G>A , CM000663.1:g.207648416G>A	GRCh37
NC_000001.9:g.205715039G>A	NCBI36
NG_013006.1:g.25772G>A , LRG_348:g.25772G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001006658.3:c.2571G>A MANE Select	NP_001006659.1:p.Lys857=
ENST00000367057.8:c.2571G>A MANE Select	ENSP00000356024.3:p.Lys857=
NM_001006658.2:c.2571G>A , LRG_348t1:c.2571G>A	NP_001006659.1:p.Lys857=
NM_001877.4:c.2394G>A	NP_001868.2:p.Lys798=
NM_001877.5:c.2394G>A	NP_001868.2:p.Lys798=
ENST00000367057.7:c.2571G>A	ENSP00000356024.3:p.Lys857=
ENST00000367058.7:c.2394G>A	ENSP00000356025.3:p.Lys798=
ENST00000367059.3:c.2394G>A	ENSP00000356026.3:p.Lys798=
ENST00000699620.1:c.2025G>A	ENSP00000514480.1:p.Lys675=
ENST00000699621.1:c.2014G>A
XM_011509206.1:c.2202G>A	XP_011507508.1:p.Lys734=
XM_011509206.3:c.2202G>A	XP_011507508.1:p.Lys734=