Canonical Allele Identifier: CA1322149743

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870631G= , CM000664.2:g.203870631G=	GRCh38
NC_000002.11:g.204735354G= , CM000664.1:g.204735354G=	GRCh37
NC_000002.10:g.204443599G=	NCBI36
NG_011502.1:g.7846G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.155G=	ENSP00000512353.1:p.Gly52=
ENST00000696479.1:c.227G=	ENSP00000512655.1:p.Gly76=
ENST00000427473.3:n.189G=
ENST00000648405.2:c.155G= MANE Select	ENSP00000497102.1:p.Gly52=
ENST00000650075.1:n.179G=
ENST00000295854.10:c.155G=	ENSP00000295854.6:p.Gly52=
ENST00000302823.7:c.155G=	ENSP00000303939.3:p.Gly52=
ENST00000427473.2:c.44G=	ENSP00000409707.2:p.Gly15=
ENST00000472206.1:c.155G=	ENSP00000417779.1:p.Gly52=
ENST00000487393.1:n.110-2077G=
NM_001037631.2:c.155G=	NP_001032720.1:p.Gly52=
NM_005214.4:c.155G=	NP_005205.2:p.Gly52=
XR_241294.1:n.295G=
NM_001037631.3:c.155G=	NP_001032720.1:p.Gly52=
NM_005214.5:c.155G= MANE Select	NP_005205.2:p.Gly52=