Canonical Allele Identifier: CA2003456957
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339710_118339715delinsACACAC , CM000673.2:g.118339710_118339715delinsACACAC GRCh38
NC_000011.9:g.118210425_118210430delinsACACAC , CM000673.1:g.118210425_118210430delinsACACAC GRCh37
NC_000011.8:g.117715635_117715640delinsACACAC NCBI36
NG_007566.1:g.367_372delinsACACAC , LRG_39:g.367_372delinsACACAC
NG_009891.1:g.8030_8035delinsGTGTGT , LRG_37:g.8030_8035delinsGTGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.953_958delinsGTGTGT
ENST00000695667.1:n.471_476delinsGTGTGT
ENST00000300692.9:c.406+60_406+65delinsGTGTGT MANE Select ENSP00000300692.4:n.406+60_406+65delinsGTGTGT
ENST00000300692.8:c.406+60_406+65delinsGTGTGT ENSP00000300692.4:n.406+60_406+65delinsGTGTGT
ENST00000392884.2:c.275-221_275-216delinsGTGTGT ENSP00000376622.2:n.275-221_275-216delinsGTGTGT
ENST00000526561.1:n.80-221_80-216delinsGTGTGT
ENST00000529594.5:c.187+60_187+65delinsGTGTGT ENSP00000437335.1:n.187+60_187+65delinsGTGTGT
ENST00000534687.5:c.288-221_288-216delinsGTGTGT
NM_000732.4:c.406+60_406+65delinsGTGTGT , LRG_37t1:c.406+60_406+65delinsGTGTGT NP_000723.1:n.406+60_406+65delinsGTGTGT
NM_001040651.1:c.275-221_275-216delinsGTGTGT NP_001035741.1:n.275-221_275-216delinsGTGTGT
NM_001040651.2:c.275-221_275-216delinsGTGTGT NP_001035741.1:n.275-221_275-216delinsGTGTGT
NM_000732.6:c.406+60_406+65delinsGTGTGT MANE Select NP_000723.1:n.406+60_406+65delinsGTGTGT