Canonical Allele Identifier: CA2616232438

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339738-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339739del , CM000673.2:g.118339739del	GRCh38
NC_000011.9:g.118210454del , CM000673.1:g.118210454del	GRCh37
NC_000011.8:g.117715664del	NCBI36
NG_007566.1:g.396del , LRG_39:g.396del
NG_009891.1:g.8006del , LRG_37:g.8006del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.929del
ENST00000695667.1:n.447del
ENST00000695668.1:n.2427del
ENST00000300692.9:c.406+36del MANE Select	ENSP00000300692.4:n.406+36del
ENST00000300692.8:c.406+36del	ENSP00000300692.4:n.406+36del
ENST00000392884.2:c.275-245del	ENSP00000376622.2:n.275-245del
ENST00000526561.1:n.80-245del
ENST00000529594.5:c.187+36del	ENSP00000437335.1:n.187+36del
ENST00000534687.5:c.288-245del
NM_000732.4:c.406+36del , LRG_37t1:c.406+36del	NP_000723.1:n.406+36del
NM_001040651.1:c.275-245del	NP_001035741.1:n.275-245del
NM_001040651.2:c.275-245del	NP_001035741.1:n.275-245del
NM_000732.6:c.406+36del MANE Select	NP_000723.1:n.406+36del