Canonical Allele Identifier: CA1322150081
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871399C= , CM000664.2:g.203871399C= GRCh38
NC_000002.11:g.204736122C= , CM000664.1:g.204736122C= GRCh37
NC_000002.10:g.204444367C= NCBI36
NG_011502.1:g.8614C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.479C= ENSP00000512353.1:p.Ser160=
ENST00000696479.1:c.551C= ENSP00000512655.1:p.Ser184=
ENST00000427473.3:n.491+466C=
ENST00000648405.2:c.479C= MANE Select ENSP00000497102.1:p.Ser160=
ENST00000650075.1:n.503C=
ENST00000295854.10:c.457+466C= ENSP00000295854.6:n.457+466C=
ENST00000302823.7:c.479C= ENSP00000303939.3:p.Ser160=
ENST00000427473.2:c.346+466C= ENSP00000409707.2:n.346+466C=
ENST00000472206.1:c.172+751C= ENSP00000417779.1:n.172+751C=
ENST00000487393.1:n.110-1309C=
NM_001037631.2:c.457+466C= NP_001032720.1:n.457+466C=
NM_005214.4:c.479C= NP_005205.2:p.Ser160=
XR_241294.1:n.619C=
NM_001037631.3:c.457+466C= NP_001032720.1:n.457+466C=
NM_005214.5:c.479C= MANE Select NP_005205.2:p.Ser160=