Canonical Allele Identifier: CA2725025489

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059133

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339724_118339725insAACA , CM000673.2:g.118339724_118339725insAACA	GRCh38
NC_000011.9:g.118210439_118210440insAACA , CM000673.1:g.118210439_118210440insAACA	GRCh37
NC_000011.8:g.117715649_117715650insAACA	NCBI36
NG_007566.1:g.381_382insAACA , LRG_39:g.381_382insAACA
NG_009891.1:g.8023_8024insTTGT , LRG_37:g.8023_8024insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.946_947insTTGT
ENST00000695667.1:n.464_465insTTGT
ENST00000300692.9:c.406+53_406+54insTTGT MANE Select	ENSP00000300692.4:n.406+53_406+54insTTGT
ENST00000300692.8:c.406+53_406+54insTTGT	ENSP00000300692.4:n.406+53_406+54insTTGT
ENST00000392884.2:c.275-228_275-227insTTGT	ENSP00000376622.2:n.275-228_275-227insTTGT
ENST00000526561.1:n.80-228_80-227insTTGT
ENST00000529594.5:c.187+53_187+54insTTGT	ENSP00000437335.1:n.187+53_187+54insTTGT
ENST00000534687.5:c.288-228_288-227insTTGT
NM_000732.4:c.406+53_406+54insTTGT , LRG_37t1:c.406+53_406+54insTTGT	NP_000723.1:n.406+53_406+54insTTGT
NM_001040651.1:c.275-228_275-227insTTGT	NP_001035741.1:n.275-228_275-227insTTGT
NM_001040651.2:c.275-228_275-227insTTGT	NP_001035741.1:n.275-228_275-227insTTGT
NM_000732.6:c.406+53_406+54insTTGT MANE Select	NP_000723.1:n.406+53_406+54insTTGT