Canonical Allele Identifier: CA1322154007
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871511C= , CM000664.2:g.203871511C= GRCh38
NC_000002.11:g.204736234C= , CM000664.1:g.204736234C= GRCh37
NC_000002.10:g.204444479C= NCBI36
NG_011502.1:g.8726C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.507+84C= ENSP00000512353.1:n.507+84C=
ENST00000696479.1:c.639+24C= ENSP00000512655.1:n.639+24C=
ENST00000427473.3:n.491+578C=
ENST00000648405.2:c.567+24C= MANE Select ENSP00000497102.1:n.567+24C=
ENST00000650075.1:n.591+24C=
ENST00000295854.10:c.457+578C= ENSP00000295854.6:n.457+578C=
ENST00000302823.7:c.567+24C= ENSP00000303939.3:n.567+24C=
ENST00000427473.2:c.346+578C= ENSP00000409707.2:n.346+578C=
ENST00000472206.1:c.172+863C= ENSP00000417779.1:n.172+863C=
ENST00000487393.1:n.110-1197C=
NM_001037631.2:c.457+578C= NP_001032720.1:n.457+578C=
NM_005214.4:c.567+24C= NP_005205.2:n.567+24C=
XR_241294.1:n.707+24C=
NM_001037631.3:c.457+578C= NP_001032720.1:n.457+578C=
NM_005214.5:c.567+24C= MANE Select NP_005205.2:n.567+24C=