Canonical Allele Identifier: CA1322148604

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203868002G= , CM000664.2:g.203868002G=	GRCh38
NC_000002.11:g.204732725G= , CM000664.1:g.204732725G=	GRCh37
NC_000002.10:g.204440970G=	NCBI36
NG_011502.1:g.5217G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696049.1:c.60G=	ENSP00000512353.1:p.Trp20=
ENST00000696479.1:c.132G=	ENSP00000512655.1:p.Trp44=
ENST00000648405.2:c.60G= MANE Select	ENSP00000497102.1:p.Trp20=
ENST00000295854.10:c.60G=	ENSP00000295854.6:p.Trp20=
ENST00000302823.7:c.60G=	ENSP00000303939.3:p.Trp20=
ENST00000472206.1:c.60G=	ENSP00000417779.1:p.Trp20=
ENST00000487393.1:n.60G=
NM_001037631.2:c.60G=	NP_001032720.1:p.Trp20=
NM_005214.4:c.60G=	NP_005205.2:p.Trp20=
XR_241294.1:n.200G=
NM_001037631.3:c.60G=	NP_001032720.1:p.Trp20=
NM_005214.5:c.60G= MANE Select	NP_005205.2:p.Trp20=