Canonical Allele Identifier: CA2616232412

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339711-C-CACAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339714_118339715insGACA , CM000673.2:g.118339714_118339715insGACA	GRCh38
NC_000011.9:g.118210429_118210430insGACA , CM000673.1:g.118210429_118210430insGACA	GRCh37
NC_000011.8:g.117715639_117715640insGACA	NCBI36
NG_007566.1:g.371_372insGACA , LRG_39:g.371_372insGACA
NG_009891.1:g.8033_8034insCTGT , LRG_37:g.8033_8034insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.956_957insCTGT
ENST00000695667.1:n.474_475insCTGT
ENST00000300692.9:c.406+63_406+64insCTGT MANE Select	ENSP00000300692.4:n.406+63_406+64insCTGT
ENST00000300692.8:c.406+63_406+64insCTGT	ENSP00000300692.4:n.406+63_406+64insCTGT
ENST00000392884.2:c.275-218_275-217insCTGT	ENSP00000376622.2:n.275-218_275-217insCTGT
ENST00000526561.1:n.80-218_80-217insCTGT
ENST00000529594.5:c.187+63_187+64insCTGT	ENSP00000437335.1:n.187+63_187+64insCTGT
ENST00000534687.5:c.288-218_288-217insCTGT
NM_000732.4:c.406+63_406+64insCTGT , LRG_37t1:c.406+63_406+64insCTGT	NP_000723.1:n.406+63_406+64insCTGT
NM_001040651.1:c.275-218_275-217insCTGT	NP_001035741.1:n.275-218_275-217insCTGT
NM_001040651.2:c.275-218_275-217insCTGT	NP_001035741.1:n.275-218_275-217insCTGT
NM_000732.6:c.406+63_406+64insCTGT MANE Select	NP_000723.1:n.406+63_406+64insCTGT