Canonical Allele Identifier: CA1322150080
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871396A= , CM000664.2:g.203871396A= GRCh38
NC_000002.11:g.204736119A= , CM000664.1:g.204736119A= GRCh37
NC_000002.10:g.204444364A= NCBI36
NG_011502.1:g.8611A=

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.476A= ENSP00000512353.1:p.Asp159=
ENST00000696479.1:c.548A= ENSP00000512655.1:p.Asp183=
ENST00000427473.3:n.491+463A=
ENST00000648405.2:c.476A= MANE Select ENSP00000497102.1:p.Asp159=
ENST00000650075.1:n.500A=
ENST00000295854.10:c.457+463A= ENSP00000295854.6:n.457+463A=
ENST00000302823.7:c.476A= ENSP00000303939.3:p.Asp159=
ENST00000427473.2:c.346+463A= ENSP00000409707.2:n.346+463A=
ENST00000472206.1:c.172+748A= ENSP00000417779.1:n.172+748A=
ENST00000487393.1:n.110-1312A=
NM_001037631.2:c.457+463A= NP_001032720.1:n.457+463A=
NM_005214.4:c.476A= NP_005205.2:p.Asp159=
XR_241294.1:n.616A=
NM_001037631.3:c.457+463A= NP_001032720.1:n.457+463A=
NM_005214.5:c.476A= MANE Select NP_005205.2:p.Asp159=