Canonical Allele Identifier: CA2725026618

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059173

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339738_118339739insAACA , CM000673.2:g.118339738_118339739insAACA	GRCh38
NC_000011.9:g.118210453_118210454insAACA , CM000673.1:g.118210453_118210454insAACA	GRCh37
NC_000011.8:g.117715663_117715664insAACA	NCBI36
NG_007566.1:g.395_396insAACA , LRG_39:g.395_396insAACA
NG_009891.1:g.8009_8010insTTGT , LRG_37:g.8009_8010insTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.932_933insTTGT
ENST00000695667.1:n.450_451insTTGT
ENST00000695668.1:n.2430_2431insTTGT
ENST00000300692.9:c.406+39_406+40insTTGT MANE Select	ENSP00000300692.4:n.406+39_406+40insTTGT
ENST00000300692.8:c.406+39_406+40insTTGT	ENSP00000300692.4:n.406+39_406+40insTTGT
ENST00000392884.2:c.275-242_275-241insTTGT	ENSP00000376622.2:n.275-242_275-241insTTGT
ENST00000526561.1:n.80-242_80-241insTTGT
ENST00000529594.5:c.187+39_187+40insTTGT	ENSP00000437335.1:n.187+39_187+40insTTGT
ENST00000534687.5:c.288-242_288-241insTTGT
NM_000732.4:c.406+39_406+40insTTGT , LRG_37t1:c.406+39_406+40insTTGT	NP_000723.1:n.406+39_406+40insTTGT
NM_001040651.1:c.275-242_275-241insTTGT	NP_001035741.1:n.275-242_275-241insTTGT
NM_001040651.2:c.275-242_275-241insTTGT	NP_001035741.1:n.275-242_275-241insTTGT
NM_000732.6:c.406+39_406+40insTTGT MANE Select	NP_000723.1:n.406+39_406+40insTTGT