Canonical Allele Identifier: CA1322150079
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203871393C= , CM000664.2:g.203871393C= GRCh38
NC_000002.11:g.204736116C= , CM000664.1:g.204736116C= GRCh37
NC_000002.10:g.204444361C= NCBI36
NG_011502.1:g.8608C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.473C= ENSP00000512353.1:p.Pro158=
ENST00000696479.1:c.545C= ENSP00000512655.1:p.Pro182=
ENST00000427473.3:n.491+460C=
ENST00000648405.2:c.473C= MANE Select ENSP00000497102.1:p.Pro158=
ENST00000650075.1:n.497C=
ENST00000295854.10:c.457+460C= ENSP00000295854.6:n.457+460C=
ENST00000302823.7:c.473C= ENSP00000303939.3:p.Pro158=
ENST00000427473.2:c.346+460C= ENSP00000409707.2:n.346+460C=
ENST00000472206.1:c.172+745C= ENSP00000417779.1:n.172+745C=
ENST00000487393.1:n.110-1315C=
NM_001037631.2:c.457+460C= NP_001032720.1:n.457+460C=
NM_005214.4:c.473C= NP_005205.2:p.Pro158=
XR_241294.1:n.613C=
NM_001037631.3:c.457+460C= NP_001032720.1:n.457+460C=
NM_005214.5:c.473C= MANE Select NP_005205.2:p.Pro158=