Canonical Allele Identifier: CA1322149995

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871231C= , CM000664.2:g.203871231C=	GRCh38
NC_000002.11:g.204735954C= , CM000664.1:g.204735954C=	GRCh37
NC_000002.10:g.204444199C=	NCBI36
NG_011502.1:g.8446C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.458-147C=	ENSP00000512353.1:n.458-147C=
ENST00000696479.1:c.530-147C=	ENSP00000512655.1:n.530-147C=
ENST00000427473.3:n.491+298C=
ENST00000648405.2:c.458-147C= MANE Select	ENSP00000497102.1:n.458-147C=
ENST00000650075.1:n.482-147C=
ENST00000295854.10:c.457+298C=	ENSP00000295854.6:n.457+298C=
ENST00000302823.7:c.458-147C=	ENSP00000303939.3:n.458-147C=
ENST00000427473.2:c.346+298C=	ENSP00000409707.2:n.346+298C=
ENST00000472206.1:c.172+583C=	ENSP00000417779.1:n.172+583C=
ENST00000487393.1:n.110-1477C=
NM_001037631.2:c.457+298C=	NP_001032720.1:n.457+298C=
NM_005214.4:c.458-147C=	NP_005205.2:n.458-147C=
XR_241294.1:n.598-147C=
NM_001037631.3:c.457+298C=	NP_001032720.1:n.457+298C=
NM_005214.5:c.458-147C= MANE Select	NP_005205.2:n.458-147C=