Canonical Allele Identifier: CA1322148597

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203867991A= , CM000664.2:g.203867991A=	GRCh38
NC_000002.11:g.204732714A= , CM000664.1:g.204732714A=	GRCh37
NC_000002.10:g.204440959A=	NCBI36
NG_011502.1:g.5206A=

Transcript Alleles

HGVS	Amino-acid Change
NM_005214.5:c.49A= MANE Select	NP_005205.2:p.Thr17=
ENST00000648405.2:c.49A= MANE Select	ENSP00000497102.1:p.Thr17=
NM_001037631.2:c.49A=	NP_001032720.1:p.Thr17=
NM_001037631.3:c.49A=	NP_001032720.1:p.Thr17=
NM_005214.4:c.49A=	NP_005205.2:p.Thr17=
ENST00000295854.10:c.49A=	ENSP00000295854.6:p.Thr17=
ENST00000302823.7:c.49A=	ENSP00000303939.3:p.Thr17=
ENST00000472206.1:c.49A=	ENSP00000417779.1:p.Thr17=
ENST00000487393.1:n.49A=
ENST00000696049.1:c.49A=	ENSP00000512353.1:p.Thr17=
ENST00000696479.1:c.121A=	ENSP00000512655.1:p.Thr41=
XR_241294.1:n.189A=