Canonical Allele Identifier: CA2725025445

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059084

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339716_118339717insGACA , CM000673.2:g.118339716_118339717insGACA	GRCh38
NC_000011.9:g.118210431_118210432insGACA , CM000673.1:g.118210431_118210432insGACA	GRCh37
NC_000011.8:g.117715641_117715642insGACA	NCBI36
NG_007566.1:g.373_374insGACA , LRG_39:g.373_374insGACA
NG_009891.1:g.8031_8032insCTGT , LRG_37:g.8031_8032insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.954_955insCTGT
ENST00000695667.1:n.472_473insCTGT
ENST00000300692.9:c.406+61_406+62insCTGT MANE Select	ENSP00000300692.4:n.406+61_406+62insCTGT
ENST00000300692.8:c.406+61_406+62insCTGT	ENSP00000300692.4:n.406+61_406+62insCTGT
ENST00000392884.2:c.275-220_275-219insCTGT	ENSP00000376622.2:n.275-220_275-219insCTGT
ENST00000526561.1:n.80-220_80-219insCTGT
ENST00000529594.5:c.187+61_187+62insCTGT	ENSP00000437335.1:n.187+61_187+62insCTGT
ENST00000534687.5:c.288-220_288-219insCTGT
NM_000732.4:c.406+61_406+62insCTGT , LRG_37t1:c.406+61_406+62insCTGT	NP_000723.1:n.406+61_406+62insCTGT
NM_001040651.1:c.275-220_275-219insCTGT	NP_001035741.1:n.275-220_275-219insCTGT
NM_001040651.2:c.275-220_275-219insCTGT	NP_001035741.1:n.275-220_275-219insCTGT
NM_000732.6:c.406+61_406+62insCTGT MANE Select	NP_000723.1:n.406+61_406+62insCTGT