Canonical Allele Identifier: CA1322149763

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203870684C= , CM000664.2:g.203870684C=	GRCh38
NC_000002.11:g.204735407C= , CM000664.1:g.204735407C=	GRCh37
NC_000002.10:g.204443652C=	NCBI36
NG_011502.1:g.7899C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.208C=	ENSP00000512353.1:p.Arg70=
ENST00000696479.1:c.280C=	ENSP00000512655.1:p.Arg94=
ENST00000427473.3:n.242C=
ENST00000648405.2:c.208C= MANE Select	ENSP00000497102.1:p.Arg70=
ENST00000650075.1:n.232C=
ENST00000295854.10:c.208C=	ENSP00000295854.6:p.Arg70=
ENST00000302823.7:c.208C=	ENSP00000303939.3:p.Arg70=
ENST00000427473.2:c.97C=	ENSP00000409707.2:p.Arg33=
ENST00000472206.1:c.172+36C=	ENSP00000417779.1:n.172+36C=
ENST00000487393.1:n.110-2024C=
NM_001037631.2:c.208C=	NP_001032720.1:p.Arg70=
NM_005214.4:c.208C=	NP_005205.2:p.Arg70=
XR_241294.1:n.348C=
NM_001037631.3:c.208C=	NP_001032720.1:p.Arg70=
NM_005214.5:c.208C= MANE Select	NP_005205.2:p.Arg70=