Canonical Allele Identifier: CA2616232408
Gene: CD3D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339710_118339711insGACACA , CM000673.2:g.118339710_118339711insGACACA GRCh38
NC_000011.9:g.118210425_118210426insGACACA , CM000673.1:g.118210425_118210426insGACACA GRCh37
NC_000011.8:g.117715635_117715636insGACACA NCBI36
NG_007566.1:g.367_368insGACACA , LRG_39:g.367_368insGACACA
NG_009891.1:g.8035_8036insGTGTCT , LRG_37:g.8035_8036insGTGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.958_959insGTGTCT
ENST00000695667.1:n.476_477insGTGTCT
ENST00000300692.9:c.406+65_406+66insGTGTCT MANE Select ENSP00000300692.4:n.406+65_406+66insGTGTCT
ENST00000300692.8:c.406+65_406+66insGTGTCT ENSP00000300692.4:n.406+65_406+66insGTGTCT
ENST00000392884.2:c.275-216_275-215insGTGTCT ENSP00000376622.2:n.275-216_275-215insGTGTCT
ENST00000526561.1:n.80-216_80-215insGTGTCT
ENST00000529594.5:c.187+65_187+66insGTGTCT ENSP00000437335.1:n.187+65_187+66insGTGTCT
ENST00000534687.5:c.288-216_288-215insGTGTCT
NM_000732.4:c.406+65_406+66insGTGTCT , LRG_37t1:c.406+65_406+66insGTGTCT NP_000723.1:n.406+65_406+66insGTGTCT
NM_001040651.1:c.275-216_275-215insGTGTCT NP_001035741.1:n.275-216_275-215insGTGTCT
NM_001040651.2:c.275-216_275-215insGTGTCT NP_001035741.1:n.275-216_275-215insGTGTCT
NM_000732.6:c.406+65_406+66insGTGTCT MANE Select NP_000723.1:n.406+65_406+66insGTGTCT