Canonical Allele Identifier: CA2003456977

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339731_118339743delinsCACACACACACAA , CM000673.2:g.118339731_118339743delinsCACACACACACAA	GRCh38
NC_000011.9:g.118210446_118210458delinsCACACACACACAA , CM000673.1:g.118210446_118210458delinsCACACACACACAA	GRCh37
NC_000011.8:g.117715656_117715668delinsCACACACACACAA	NCBI36
NG_007566.1:g.388_400delinsCACACACACACAA , LRG_39:g.388_400delinsCACACACACACAA
NG_009891.1:g.8002_8014delinsTTGTGTGTGTGTG , LRG_37:g.8002_8014delinsTTGTGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.925_937delinsTTGTGTGTGTGTG
ENST00000695667.1:n.443_455delinsTTGTGTGTGTGTG
ENST00000695668.1:n.2423_2435delinsTTGTGTGTGTGTG
ENST00000300692.9:c.406+32_406+44delinsTTGTGTGTGTGTG MANE Select	ENSP00000300692.4:n.406+32_406+44delinsTTGTGTGTGTGTG
ENST00000300692.8:c.406+32_406+44delinsTTGTGTGTGTGTG	ENSP00000300692.4:n.406+32_406+44delinsTTGTGTGTGTGTG
ENST00000392884.2:c.275-249_275-237delinsTTGTGTGTGTGTG	ENSP00000376622.2:n.275-249_275-237delinsTTGTGTGTGTGTG
ENST00000526561.1:n.80-249_80-237delinsTTGTGTGTGTGTG
ENST00000529594.5:c.187+32_187+44delinsTTGTGTGTGTGTG	ENSP00000437335.1:n.187+32_187+44delinsTTGTGTGTGTGTG
ENST00000534687.5:c.288-249_288-237delinsTTGTGTGTGTGTG
NM_000732.4:c.406+32_406+44delinsTTGTGTGTGTGTG , LRG_37t1:c.406+32_406+44delinsTTGTGTGTGTGTG	NP_000723.1:n.406+32_406+44delinsTTGTGTGTGTGTG
NM_001040651.1:c.275-249_275-237delinsTTGTGTGTGTGTG	NP_001035741.1:n.275-249_275-237delinsTTGTGTGTGTGTG
NM_001040651.2:c.275-249_275-237delinsTTGTGTGTGTGTG	NP_001035741.1:n.275-249_275-237delinsTTGTGTGTGTGTG
NM_000732.6:c.406+32_406+44delinsTTGTGTGTGTGTG MANE Select	NP_000723.1:n.406+32_406+44delinsTTGTGTGTGTGTG