Canonical Allele Identifier: CA2003456988

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339739_118339743delinsCACAA , CM000673.2:g.118339739_118339743delinsCACAA	GRCh38
NC_000011.9:g.118210454_118210458delinsCACAA , CM000673.1:g.118210454_118210458delinsCACAA	GRCh37
NC_000011.8:g.117715664_117715668delinsCACAA	NCBI36
NG_007566.1:g.396_400delinsCACAA , LRG_39:g.396_400delinsCACAA
NG_009891.1:g.8002_8006delinsTTGTG , LRG_37:g.8002_8006delinsTTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.925_929delinsTTGTG
ENST00000695667.1:n.443_447delinsTTGTG
ENST00000695668.1:n.2423_2427delinsTTGTG
ENST00000300692.9:c.406+32_406+36delinsTTGTG MANE Select	ENSP00000300692.4:n.406+32_406+36delinsTTGTG
ENST00000300692.8:c.406+32_406+36delinsTTGTG	ENSP00000300692.4:n.406+32_406+36delinsTTGTG
ENST00000392884.2:c.275-249_275-245delinsTTGTG	ENSP00000376622.2:n.275-249_275-245delinsTTGTG
ENST00000526561.1:n.80-249_80-245delinsTTGTG
ENST00000529594.5:c.187+32_187+36delinsTTGTG	ENSP00000437335.1:n.187+32_187+36delinsTTGTG
ENST00000534687.5:c.288-249_288-245delinsTTGTG
NM_000732.4:c.406+32_406+36delinsTTGTG , LRG_37t1:c.406+32_406+36delinsTTGTG	NP_000723.1:n.406+32_406+36delinsTTGTG
NM_001040651.1:c.275-249_275-245delinsTTGTG	NP_001035741.1:n.275-249_275-245delinsTTGTG
NM_001040651.2:c.275-249_275-245delinsTTGTG	NP_001035741.1:n.275-249_275-245delinsTTGTG
NM_000732.6:c.406+32_406+36delinsTTGTG MANE Select	NP_000723.1:n.406+32_406+36delinsTTGTG