Canonical Allele Identifier: CA2724938364

Gene: CD3D

Linked Data

• dbSNP Id: rs57470363

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339742_118339743insCACACAAA , CM000673.2:g.118339742_118339743insCACACAAA	GRCh38
NC_000011.9:g.118210457_118210458insCACACAAA , CM000673.1:g.118210457_118210458insCACACAAA	GRCh37
NC_000011.8:g.117715667_117715668insCACACAAA	NCBI36
NG_007566.1:g.399_400insCACACAAA , LRG_39:g.399_400insCACACAAA
NG_009891.1:g.8003_8004insTTGTGTGT , LRG_37:g.8003_8004insTTGTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.926_927insTTGTGTGT
ENST00000695667.1:n.444_445insTTGTGTGT
ENST00000695668.1:n.2424_2425insTTGTGTGT
ENST00000300692.9:c.406+33_406+34insTTGTGTGT MANE Select	ENSP00000300692.4:n.406+33_406+34insTTGTGTGT
ENST00000300692.8:c.406+33_406+34insTTGTGTGT	ENSP00000300692.4:n.406+33_406+34insTTGTGTGT
ENST00000392884.2:c.275-248_275-247insTTGTGTGT	ENSP00000376622.2:n.275-248_275-247insTTGTGTGT
ENST00000526561.1:n.80-248_80-247insTTGTGTGT
ENST00000529594.5:c.187+33_187+34insTTGTGTGT	ENSP00000437335.1:n.187+33_187+34insTTGTGTGT
ENST00000534687.5:c.288-248_288-247insTTGTGTGT
NM_000732.4:c.406+33_406+34insTTGTGTGT , LRG_37t1:c.406+33_406+34insTTGTGTGT	NP_000723.1:n.406+33_406+34insTTGTGTGT
NM_001040651.1:c.275-248_275-247insTTGTGTGT	NP_001035741.1:n.275-248_275-247insTTGTGTGT
NM_001040651.2:c.275-248_275-247insTTGTGTGT	NP_001035741.1:n.275-248_275-247insTTGTGTGT
NM_000732.6:c.406+33_406+34insTTGTGTGT MANE Select	NP_000723.1:n.406+33_406+34insTTGTGTGT