Canonical Allele Identifier: CA2003456981

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339733_118339743delinsCACACACACAA , CM000673.2:g.118339733_118339743delinsCACACACACAA	GRCh38
NC_000011.9:g.118210448_118210458delinsCACACACACAA , CM000673.1:g.118210448_118210458delinsCACACACACAA	GRCh37
NC_000011.8:g.117715658_117715668delinsCACACACACAA	NCBI36
NG_007566.1:g.390_400delinsCACACACACAA , LRG_39:g.390_400delinsCACACACACAA
NG_009891.1:g.8002_8012delinsTTGTGTGTGTG , LRG_37:g.8002_8012delinsTTGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.925_935delinsTTGTGTGTGTG
ENST00000695667.1:n.443_453delinsTTGTGTGTGTG
ENST00000695668.1:n.2423_2433delinsTTGTGTGTGTG
ENST00000300692.9:c.406+32_406+42delinsTTGTGTGTGTG MANE Select	ENSP00000300692.4:n.406+32_406+42delinsTTGTGTGTGTG
ENST00000300692.8:c.406+32_406+42delinsTTGTGTGTGTG	ENSP00000300692.4:n.406+32_406+42delinsTTGTGTGTGTG
ENST00000392884.2:c.275-249_275-239delinsTTGTGTGTGTG	ENSP00000376622.2:n.275-249_275-239delinsTTGTGTGTGTG
ENST00000526561.1:n.80-249_80-239delinsTTGTGTGTGTG
ENST00000529594.5:c.187+32_187+42delinsTTGTGTGTGTG	ENSP00000437335.1:n.187+32_187+42delinsTTGTGTGTGTG
ENST00000534687.5:c.288-249_288-239delinsTTGTGTGTGTG
NM_000732.4:c.406+32_406+42delinsTTGTGTGTGTG , LRG_37t1:c.406+32_406+42delinsTTGTGTGTGTG	NP_000723.1:n.406+32_406+42delinsTTGTGTGTGTG
NM_001040651.1:c.275-249_275-239delinsTTGTGTGTGTG	NP_001035741.1:n.275-249_275-239delinsTTGTGTGTGTG
NM_001040651.2:c.275-249_275-239delinsTTGTGTGTGTG	NP_001035741.1:n.275-249_275-239delinsTTGTGTGTGTG
NM_000732.6:c.406+32_406+42delinsTTGTGTGTGTG MANE Select	NP_000723.1:n.406+32_406+42delinsTTGTGTGTGTG