Canonical Allele Identifier: CA2003456966
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339720_118339721delinsAC , CM000673.2:g.118339720_118339721delinsAC GRCh38
NC_000011.9:g.118210435_118210436delinsAC , CM000673.1:g.118210435_118210436delinsAC GRCh37
NC_000011.8:g.117715645_117715646delinsAC NCBI36
NG_007566.1:g.377_378delinsAC , LRG_39:g.377_378delinsAC
NG_009891.1:g.8024_8025delinsGT , LRG_37:g.8024_8025delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.947_948delinsGT
ENST00000695667.1:n.465_466delinsGT
ENST00000300692.9:c.406+54_406+55delinsGT MANE Select ENSP00000300692.4:n.406+54_406+55delinsGT
ENST00000300692.8:c.406+54_406+55delinsGT ENSP00000300692.4:n.406+54_406+55delinsGT
ENST00000392884.2:c.275-227_275-226delinsGT ENSP00000376622.2:n.275-227_275-226delinsGT
ENST00000526561.1:n.80-227_80-226delinsGT
ENST00000529594.5:c.187+54_187+55delinsGT ENSP00000437335.1:n.187+54_187+55delinsGT
ENST00000534687.5:c.288-227_288-226delinsGT
NM_000732.4:c.406+54_406+55delinsGT , LRG_37t1:c.406+54_406+55delinsGT NP_000723.1:n.406+54_406+55delinsGT
NM_001040651.1:c.275-227_275-226delinsGT NP_001035741.1:n.275-227_275-226delinsGT
NM_001040651.2:c.275-227_275-226delinsGT NP_001035741.1:n.275-227_275-226delinsGT
NM_000732.6:c.406+54_406+55delinsGT MANE Select NP_000723.1:n.406+54_406+55delinsGT