Canonical Allele Identifier: CA2568715973
Gene: CTLA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203868009_203868010insG , CM000664.2:g.203868009_203868010insG GRCh38
NC_000002.11:g.204732732_204732733insG , CM000664.1:g.204732732_204732733insG GRCh37
NC_000002.10:g.204440977_204440978insG NCBI36
NG_011502.1:g.5224_5225insG

Transcript Alleles

HGVS Amino-acid change
ENST00000696049.1:c.67_68insG ENSP00000512353.1:p.Thr23SerfsTer?
ENST00000696479.1:c.139_140insG ENSP00000512655.1:p.Thr47SerfsTer?
ENST00000648405.2:c.67_68insG MANE Select ENSP00000497102.1:p.Thr23SerfsTer?
ENST00000295854.10:c.67_68insG ENSP00000295854.6:p.Thr23SerfsTer?
ENST00000302823.7:c.67_68insG ENSP00000303939.3:p.Thr23SerfsTer?
ENST00000472206.1:c.67_68insG ENSP00000417779.1:p.Thr23SerfsTer?
ENST00000487393.1:n.67_68insG
NM_001037631.2:c.67_68insG NP_001032720.1:p.Thr23SerfsTer?
NM_005214.4:c.67_68insG NP_005205.2:p.Thr23SerfsTer?
XR_241294.1:n.207_208insG
NM_001037631.3:c.67_68insG NP_001032720.1:p.Thr23SerfsTer?
NM_005214.5:c.67_68insG MANE Select NP_005205.2:p.Thr23SerfsTer?