Canonical Allele Identifier: CA2003456963
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339718_118339719delinsAC , CM000673.2:g.118339718_118339719delinsAC GRCh38
NC_000011.9:g.118210433_118210434delinsAC , CM000673.1:g.118210433_118210434delinsAC GRCh37
NC_000011.8:g.117715643_117715644delinsAC NCBI36
NG_007566.1:g.375_376delinsAC , LRG_39:g.375_376delinsAC
NG_009891.1:g.8026_8027delinsGT , LRG_37:g.8026_8027delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.949_950delinsGT
ENST00000695667.1:n.467_468delinsGT
ENST00000300692.9:c.406+56_406+57delinsGT MANE Select ENSP00000300692.4:n.406+56_406+57delinsGT
ENST00000300692.8:c.406+56_406+57delinsGT ENSP00000300692.4:n.406+56_406+57delinsGT
ENST00000392884.2:c.275-225_275-224delinsGT ENSP00000376622.2:n.275-225_275-224delinsGT
ENST00000526561.1:n.80-225_80-224delinsGT
ENST00000529594.5:c.187+56_187+57delinsGT ENSP00000437335.1:n.187+56_187+57delinsGT
ENST00000534687.5:c.288-225_288-224delinsGT
NM_000732.4:c.406+56_406+57delinsGT , LRG_37t1:c.406+56_406+57delinsGT NP_000723.1:n.406+56_406+57delinsGT
NM_001040651.1:c.275-225_275-224delinsGT NP_001035741.1:n.275-225_275-224delinsGT
NM_001040651.2:c.275-225_275-224delinsGT NP_001035741.1:n.275-225_275-224delinsGT
NM_000732.6:c.406+56_406+57delinsGT MANE Select NP_000723.1:n.406+56_406+57delinsGT