Canonical Allele Identifier: CA2003456992

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339741_118339743delinsCAA , CM000673.2:g.118339741_118339743delinsCAA	GRCh38
NC_000011.9:g.118210456_118210458delinsCAA , CM000673.1:g.118210456_118210458delinsCAA	GRCh37
NC_000011.8:g.117715666_117715668delinsCAA	NCBI36
NG_007566.1:g.398_400delinsCAA , LRG_39:g.398_400delinsCAA
NG_009891.1:g.8002_8004delinsTTG , LRG_37:g.8002_8004delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.925_927delinsTTG
ENST00000695667.1:n.443_445delinsTTG
ENST00000695668.1:n.2423_2425delinsTTG
ENST00000300692.9:c.406+32_406+34delinsTTG MANE Select	ENSP00000300692.4:n.406+32_406+34delinsTTG
ENST00000300692.8:c.406+32_406+34delinsTTG	ENSP00000300692.4:n.406+32_406+34delinsTTG
ENST00000392884.2:c.275-249_275-247delinsTTG	ENSP00000376622.2:n.275-249_275-247delinsTTG
ENST00000526561.1:n.80-249_80-247delinsTTG
ENST00000529594.5:c.187+32_187+34delinsTTG	ENSP00000437335.1:n.187+32_187+34delinsTTG
ENST00000534687.5:c.288-249_288-247delinsTTG
NM_000732.4:c.406+32_406+34delinsTTG , LRG_37t1:c.406+32_406+34delinsTTG	NP_000723.1:n.406+32_406+34delinsTTG
NM_001040651.1:c.275-249_275-247delinsTTG	NP_001035741.1:n.275-249_275-247delinsTTG
NM_001040651.2:c.275-249_275-247delinsTTG	NP_001035741.1:n.275-249_275-247delinsTTG
NM_000732.6:c.406+32_406+34delinsTTG MANE Select	NP_000723.1:n.406+32_406+34delinsTTG