Canonical Allele Identifier: CA2616232421

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339722-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339723del , CM000673.2:g.118339723del	GRCh38
NC_000011.9:g.118210438del , CM000673.1:g.118210438del	GRCh37
NC_000011.8:g.117715648del	NCBI36
NG_007566.1:g.380del , LRG_39:g.380del
NG_009891.1:g.8022del , LRG_37:g.8022del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.945del
ENST00000695667.1:n.463del
ENST00000695668.1:n.2443del
ENST00000300692.9:c.406+52del MANE Select	ENSP00000300692.4:n.406+52del
ENST00000300692.8:c.406+52del	ENSP00000300692.4:n.406+52del
ENST00000392884.2:c.275-229del	ENSP00000376622.2:n.275-229del
ENST00000526561.1:n.80-229del
ENST00000529594.5:c.187+52del	ENSP00000437335.1:n.187+52del
ENST00000534687.5:c.288-229del
NM_000732.4:c.406+52del , LRG_37t1:c.406+52del	NP_000723.1:n.406+52del
NM_001040651.1:c.275-229del	NP_001035741.1:n.275-229del
NM_001040651.2:c.275-229del	NP_001035741.1:n.275-229del
NM_000732.6:c.406+52del MANE Select	NP_000723.1:n.406+52del