Canonical Allele Identifier: CA2483404635

Gene: CR2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.207454419A= , CM000663.2:g.207454419A=	GRCh38
NC_000001.10:g.207627764A= , CM000663.1:g.207627764A=	GRCh37
NC_000001.9:g.205694387A=	NCBI36
NG_013006.1:g.5120A= , LRG_348:g.5120A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000699620.1:c.-442A=	ENSP00000514480.1:n.-442A=
ENST00000699640.1:c.-385+1324A=	ENSP00000514493.1:n.-385+1324A=
ENST00000367057.8:c.1A= MANE Select	ENSP00000356024.3:p.Met1=
ENST00000367057.7:c.1A=	ENSP00000356024.3:p.Met1=
ENST00000367058.7:c.1A=	ENSP00000356025.3:p.Met1=
ENST00000367059.3:c.1A=	ENSP00000356026.3:p.Met1=
NM_001006658.2:c.1A= , LRG_348t1:c.1A=	NP_001006659.1:p.Met1=
NM_001877.4:c.1A=	NP_001868.2:p.Met1=
NM_001006658.3:c.1A= MANE Select	NP_001006659.1:p.Met1=
NM_001877.5:c.1A=	NP_001868.2:p.Met1=