Canonical Allele Identifier: CA1322153946

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871469T= , CM000664.2:g.203871469T=	GRCh38
NC_000002.11:g.204736192T= , CM000664.1:g.204736192T=	GRCh37
NC_000002.10:g.204444437T=	NCBI36
NG_011502.1:g.8684T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+42T=	ENSP00000512353.1:n.507+42T=
ENST00000696479.1:c.621T=	ENSP00000512655.1:p.Ala207=
ENST00000427473.3:n.491+536T=
ENST00000648405.2:c.549T= MANE Select	ENSP00000497102.1:p.Ala183=
ENST00000650075.1:n.573T=
ENST00000295854.10:c.457+536T=	ENSP00000295854.6:n.457+536T=
ENST00000302823.7:c.549T=	ENSP00000303939.3:p.Ala183=
ENST00000427473.2:c.346+536T=	ENSP00000409707.2:n.346+536T=
ENST00000472206.1:c.172+821T=	ENSP00000417779.1:n.172+821T=
ENST00000487393.1:n.110-1239T=
NM_001037631.2:c.457+536T=	NP_001032720.1:n.457+536T=
NM_005214.4:c.549T=	NP_005205.2:p.Ala183=
XR_241294.1:n.689T=
NM_001037631.3:c.457+536T=	NP_001032720.1:n.457+536T=
NM_005214.5:c.549T= MANE Select	NP_005205.2:p.Ala183=