Canonical Allele Identifier: CA1322155622
Gene: CTLA4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203873950G= , CM000664.2:g.203873950G= GRCh38
NC_000002.11:g.204738673G= , CM000664.1:g.204738673G= GRCh37
NC_000002.10:g.204446918G= NCBI36
NG_011502.1:g.11165G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696479.1:c.*1138G= ENSP00000512655.1:n.*1138G=
ENST00000648405.2:c.*1138G= MANE Select ENSP00000497102.1:n.*1138G=
ENST00000302823.7:c.*1138G= ENSP00000303939.3:n.*1138G=
NM_001037631.2:c.*1175G= NP_001032720.1:n.*1175G=
NM_005214.4:c.*1138G= NP_005205.2:n.*1138G=
XR_241294.1:n.1908G=
NM_001037631.3:c.*1175G= NP_001032720.1:n.*1175G=
NM_005214.5:c.*1138G= MANE Select NP_005205.2:n.*1138G=
Search 100 bp 5'
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