Canonical Allele Identifier: CA2725026159

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059153

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339732_118339733insGACA , CM000673.2:g.118339732_118339733insGACA	GRCh38
NC_000011.9:g.118210447_118210448insGACA , CM000673.1:g.118210447_118210448insGACA	GRCh37
NC_000011.8:g.117715657_117715658insGACA	NCBI36
NG_007566.1:g.389_390insGACA , LRG_39:g.389_390insGACA
NG_009891.1:g.8015_8016insCTGT , LRG_37:g.8015_8016insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.938_939insCTGT
ENST00000695667.1:n.456_457insCTGT
ENST00000695668.1:n.2436_2437insCTGT
ENST00000300692.9:c.406+45_406+46insCTGT MANE Select	ENSP00000300692.4:n.406+45_406+46insCTGT
ENST00000300692.8:c.406+45_406+46insCTGT	ENSP00000300692.4:n.406+45_406+46insCTGT
ENST00000392884.2:c.275-236_275-235insCTGT	ENSP00000376622.2:n.275-236_275-235insCTGT
ENST00000526561.1:n.80-236_80-235insCTGT
ENST00000529594.5:c.187+45_187+46insCTGT	ENSP00000437335.1:n.187+45_187+46insCTGT
ENST00000534687.5:c.288-236_288-235insCTGT
NM_000732.4:c.406+45_406+46insCTGT , LRG_37t1:c.406+45_406+46insCTGT	NP_000723.1:n.406+45_406+46insCTGT
NM_001040651.1:c.275-236_275-235insCTGT	NP_001035741.1:n.275-236_275-235insCTGT
NM_001040651.2:c.275-236_275-235insCTGT	NP_001035741.1:n.275-236_275-235insCTGT
NM_000732.6:c.406+45_406+46insCTGT MANE Select	NP_000723.1:n.406+45_406+46insCTGT