Canonical Allele Identifier: CA1322149740

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870627C= , CM000664.2:g.203870627C=	GRCh38
NC_000002.11:g.204735350C= , CM000664.1:g.204735350C=	GRCh37
NC_000002.10:g.204443595C=	NCBI36
NG_011502.1:g.7842C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005214.5:c.151C= MANE Select	NP_005205.2:p.Arg51=
ENST00000648405.2:c.151C= MANE Select	ENSP00000497102.1:p.Arg51=
NM_001037631.2:c.151C=	NP_001032720.1:p.Arg51=
NM_001037631.3:c.151C=	NP_001032720.1:p.Arg51=
NM_005214.4:c.151C=	NP_005205.2:p.Arg51=
ENST00000295854.10:c.151C=	ENSP00000295854.6:p.Arg51=
ENST00000302823.7:c.151C=	ENSP00000303939.3:p.Arg51=
ENST00000427473.2:c.40C=	ENSP00000409707.2:p.Arg14=
ENST00000427473.3:n.185C=
ENST00000472206.1:c.151C=	ENSP00000417779.1:p.Arg51=
ENST00000487393.1:n.110-2081C=
ENST00000650075.1:n.175C=
ENST00000696049.1:c.151C=	ENSP00000512353.1:p.Arg51=
ENST00000696479.1:c.223C=	ENSP00000512655.1:p.Arg75=
XR_241294.1:n.291C=