Canonical Allele Identifier: CA1322153965

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871479A= , CM000664.2:g.203871479A=	GRCh38
NC_000002.11:g.204736202A= , CM000664.1:g.204736202A=	GRCh37
NC_000002.10:g.204444447A=	NCBI36
NG_011502.1:g.8694A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+52A=	ENSP00000512353.1:n.507+52A=
ENST00000696479.1:c.631A=	ENSP00000512655.1:p.Ser211=
ENST00000427473.3:n.491+546A=
ENST00000648405.2:c.559A= MANE Select	ENSP00000497102.1:p.Ser187=
ENST00000650075.1:n.583A=
ENST00000295854.10:c.457+546A=	ENSP00000295854.6:n.457+546A=
ENST00000302823.7:c.559A=	ENSP00000303939.3:p.Ser187=
ENST00000427473.2:c.346+546A=	ENSP00000409707.2:n.346+546A=
ENST00000472206.1:c.172+831A=	ENSP00000417779.1:n.172+831A=
ENST00000487393.1:n.110-1229A=
NM_001037631.2:c.457+546A=	NP_001032720.1:n.457+546A=
NM_005214.4:c.559A=	NP_005205.2:p.Ser187=
XR_241294.1:n.699A=
NM_001037631.3:c.457+546A=	NP_001032720.1:n.457+546A=
NM_005214.5:c.559A= MANE Select	NP_005205.2:p.Ser187=