Canonical Allele Identifier: CA2725025516

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059136

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339728_118339729insAACA , CM000673.2:g.118339728_118339729insAACA	GRCh38
NC_000011.9:g.118210443_118210444insAACA , CM000673.1:g.118210443_118210444insAACA	GRCh37
NC_000011.8:g.117715653_117715654insAACA	NCBI36
NG_007566.1:g.385_386insAACA , LRG_39:g.385_386insAACA
NG_009891.1:g.8019_8020insTTGT , LRG_37:g.8019_8020insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.942_943insTTGT
ENST00000695667.1:n.460_461insTTGT
ENST00000695668.1:n.2440_2441insTTGT
ENST00000300692.9:c.406+49_406+50insTTGT MANE Select	ENSP00000300692.4:n.406+49_406+50insTTGT
ENST00000300692.8:c.406+49_406+50insTTGT	ENSP00000300692.4:n.406+49_406+50insTTGT
ENST00000392884.2:c.275-232_275-231insTTGT	ENSP00000376622.2:n.275-232_275-231insTTGT
ENST00000526561.1:n.80-232_80-231insTTGT
ENST00000529594.5:c.187+49_187+50insTTGT	ENSP00000437335.1:n.187+49_187+50insTTGT
ENST00000534687.5:c.288-232_288-231insTTGT
NM_000732.4:c.406+49_406+50insTTGT , LRG_37t1:c.406+49_406+50insTTGT	NP_000723.1:n.406+49_406+50insTTGT
NM_001040651.1:c.275-232_275-231insTTGT	NP_001035741.1:n.275-232_275-231insTTGT
NM_001040651.2:c.275-232_275-231insTTGT	NP_001035741.1:n.275-232_275-231insTTGT
NM_000732.6:c.406+49_406+50insTTGT MANE Select	NP_000723.1:n.406+49_406+50insTTGT