Canonical Allele Identifier: CA1322148537

Gene: CTLA4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203867846C= , CM000664.2:g.203867846C=	GRCh38
NC_000002.11:g.204732569C= , CM000664.1:g.204732569C=	GRCh37
NC_000002.10:g.204440814C=	NCBI36
NG_011502.1:g.5061C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696049.1:c.-97C=	ENSP00000512353.1:n.-97C=
ENST00000696479.1:c.48-72C=	ENSP00000512655.1:n.48-72C=
ENST00000648405.2:c.-97C= MANE Select	ENSP00000497102.1:n.-97C=
ENST00000302823.7:c.-97C=	ENSP00000303939.3:n.-97C=
NM_001037631.2:c.-97C=	NP_001032720.1:n.-97C=
NM_005214.4:c.-97C=	NP_005205.2:n.-97C=
XR_241294.1:n.44C=
NM_001037631.3:c.-97C=	NP_001032720.1:n.-97C=
NM_005214.5:c.-97C= MANE Select	NP_005205.2:n.-97C=