Canonical Allele Identifier: CA2003456983

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339735_118339743delinsCACACACAA , CM000673.2:g.118339735_118339743delinsCACACACAA	GRCh38
NC_000011.9:g.118210450_118210458delinsCACACACAA , CM000673.1:g.118210450_118210458delinsCACACACAA	GRCh37
NC_000011.8:g.117715660_117715668delinsCACACACAA	NCBI36
NG_007566.1:g.392_400delinsCACACACAA , LRG_39:g.392_400delinsCACACACAA
NG_009891.1:g.8002_8010delinsTTGTGTGTG , LRG_37:g.8002_8010delinsTTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.925_933delinsTTGTGTGTG
ENST00000695667.1:n.443_451delinsTTGTGTGTG
ENST00000695668.1:n.2423_2431delinsTTGTGTGTG
ENST00000300692.9:c.406+32_406+40delinsTTGTGTGTG MANE Select	ENSP00000300692.4:n.406+32_406+40delinsTTGTGTGTG
ENST00000300692.8:c.406+32_406+40delinsTTGTGTGTG	ENSP00000300692.4:n.406+32_406+40delinsTTGTGTGTG
ENST00000392884.2:c.275-249_275-241delinsTTGTGTGTG	ENSP00000376622.2:n.275-249_275-241delinsTTGTGTGTG
ENST00000526561.1:n.80-249_80-241delinsTTGTGTGTG
ENST00000529594.5:c.187+32_187+40delinsTTGTGTGTG	ENSP00000437335.1:n.187+32_187+40delinsTTGTGTGTG
ENST00000534687.5:c.288-249_288-241delinsTTGTGTGTG
NM_000732.4:c.406+32_406+40delinsTTGTGTGTG , LRG_37t1:c.406+32_406+40delinsTTGTGTGTG	NP_000723.1:n.406+32_406+40delinsTTGTGTGTG
NM_001040651.1:c.275-249_275-241delinsTTGTGTGTG	NP_001035741.1:n.275-249_275-241delinsTTGTGTGTG
NM_001040651.2:c.275-249_275-241delinsTTGTGTGTG	NP_001035741.1:n.275-249_275-241delinsTTGTGTGTG
NM_000732.6:c.406+32_406+40delinsTTGTGTGTG MANE Select	NP_000723.1:n.406+32_406+40delinsTTGTGTGTG