Canonical Allele Identifier: CA2793810958
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339742_118339743insCCC , CM000673.2:g.118339742_118339743insCCC GRCh38
NC_000011.9:g.118210457_118210458insCCC , CM000673.1:g.118210457_118210458insCCC GRCh37
NC_000011.8:g.117715667_117715668insCCC NCBI36
NG_007566.1:g.399_400insCCC , LRG_39:g.399_400insCCC
NG_009891.1:g.8002_8003insGGG , LRG_37:g.8002_8003insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.925_926insGGG
ENST00000695667.1:n.443_444insGGG
ENST00000695668.1:n.2423_2424insGGG
ENST00000300692.9:c.406+32_406+33insGGG MANE Select ENSP00000300692.4:n.406+32_406+33insGGG
ENST00000300692.8:c.406+32_406+33insGGG ENSP00000300692.4:n.406+32_406+33insGGG
ENST00000392884.2:c.275-249_275-248insGGG ENSP00000376622.2:n.275-249_275-248insGGG
ENST00000526561.1:n.80-249_80-248insGGG
ENST00000529594.5:c.187+32_187+33insGGG ENSP00000437335.1:n.187+32_187+33insGGG
ENST00000534687.5:c.288-249_288-248insGGG
NM_000732.4:c.406+32_406+33insGGG , LRG_37t1:c.406+32_406+33insGGG NP_000723.1:n.406+32_406+33insGGG
NM_001040651.1:c.275-249_275-248insGGG NP_001035741.1:n.275-249_275-248insGGG
NM_001040651.2:c.275-249_275-248insGGG NP_001035741.1:n.275-249_275-248insGGG
NM_000732.6:c.406+32_406+33insGGG MANE Select NP_000723.1:n.406+32_406+33insGGG