Canonical Allele Identifier: CA942727045

Gene: CD3D

Linked Data

• dbSNP Id: rs1948282105
• gnomAD v3: 11-118339713-C-CAG
• gnomAD v4: 11-118339713-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339714_118339715insGA , CM000673.2:g.118339714_118339715insGA	GRCh38
NC_000011.9:g.118210429_118210430insGA , CM000673.1:g.118210429_118210430insGA	GRCh37
NC_000011.8:g.117715639_117715640insGA	NCBI36
NG_007566.1:g.371_372insGA , LRG_39:g.371_372insGA
NG_009891.1:g.8031_8032insCT , LRG_37:g.8031_8032insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.954_955insCT
ENST00000695667.1:n.472_473insCT
ENST00000300692.9:c.406+61_406+62insCT MANE Select	ENSP00000300692.4:n.406+61_406+62insCT
ENST00000300692.8:c.406+61_406+62insCT	ENSP00000300692.4:n.406+61_406+62insCT
ENST00000392884.2:c.275-220_275-219insCT	ENSP00000376622.2:n.275-220_275-219insCT
ENST00000526561.1:n.80-220_80-219insCT
ENST00000529594.5:c.187+61_187+62insCT	ENSP00000437335.1:n.187+61_187+62insCT
ENST00000534687.5:c.288-220_288-219insCT
NM_000732.4:c.406+61_406+62insCT , LRG_37t1:c.406+61_406+62insCT	NP_000723.1:n.406+61_406+62insCT
NM_001040651.1:c.275-220_275-219insCT	NP_001035741.1:n.275-220_275-219insCT
NM_001040651.2:c.275-220_275-219insCT	NP_001035741.1:n.275-220_275-219insCT
NM_000732.6:c.406+61_406+62insCT MANE Select	NP_000723.1:n.406+61_406+62insCT