Canonical Allele Identifier: CA1322154060

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203871556A= , CM000664.2:g.203871556A=	GRCh38
NC_000002.11:g.204736279A= , CM000664.1:g.204736279A=	GRCh37
NC_000002.10:g.204444524A=	NCBI36
NG_011502.1:g.8771A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.507+129A=	ENSP00000512353.1:n.507+129A=
ENST00000696479.1:c.639+69A=	ENSP00000512655.1:n.639+69A=
ENST00000427473.3:n.491+623A=
ENST00000648405.2:c.567+69A= MANE Select	ENSP00000497102.1:n.567+69A=
ENST00000650075.1:n.591+69A=
ENST00000295854.10:c.457+623A=	ENSP00000295854.6:n.457+623A=
ENST00000302823.7:c.567+69A=	ENSP00000303939.3:n.567+69A=
ENST00000427473.2:c.346+623A=	ENSP00000409707.2:n.346+623A=
ENST00000472206.1:c.172+908A=	ENSP00000417779.1:n.172+908A=
ENST00000487393.1:n.110-1152A=
NM_001037631.2:c.457+623A=	NP_001032720.1:n.457+623A=
NM_005214.4:c.567+69A=	NP_005205.2:n.567+69A=
XR_241294.1:n.707+69A=
NM_001037631.3:c.457+623A=	NP_001032720.1:n.457+623A=
NM_005214.5:c.567+69A= MANE Select	NP_005205.2:n.567+69A=