Canonical Allele Identifier: CA2616232415

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339714-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339715del , CM000673.2:g.118339715del	GRCh38
NC_000011.9:g.118210430del , CM000673.1:g.118210430del	GRCh37
NC_000011.8:g.117715640del	NCBI36
NG_007566.1:g.372del , LRG_39:g.372del
NG_009891.1:g.8030del , LRG_37:g.8030del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.953del
ENST00000695667.1:n.471del
ENST00000300692.9:c.406+60del MANE Select	ENSP00000300692.4:n.406+60del
ENST00000300692.8:c.406+60del	ENSP00000300692.4:n.406+60del
ENST00000392884.2:c.275-221del	ENSP00000376622.2:n.275-221del
ENST00000526561.1:n.80-221del
ENST00000529594.5:c.187+60del	ENSP00000437335.1:n.187+60del
ENST00000534687.5:c.288-221del
NM_000732.4:c.406+60del , LRG_37t1:c.406+60del	NP_000723.1:n.406+60del
NM_001040651.1:c.275-221del	NP_001035741.1:n.275-221del
NM_001040651.2:c.275-221del	NP_001035741.1:n.275-221del
NM_000732.6:c.406+60del MANE Select	NP_000723.1:n.406+60del