Canonical Allele Identifier: CA2616232418

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339719-C-CACAT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339722_118339723insTACA , CM000673.2:g.118339722_118339723insTACA	GRCh38
NC_000011.9:g.118210437_118210438insTACA , CM000673.1:g.118210437_118210438insTACA	GRCh37
NC_000011.8:g.117715647_117715648insTACA	NCBI36
NG_007566.1:g.379_380insTACA , LRG_39:g.379_380insTACA
NG_009891.1:g.8025_8026insATGT , LRG_37:g.8025_8026insATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.948_949insATGT
ENST00000695667.1:n.466_467insATGT
ENST00000300692.9:c.406+55_406+56insATGT MANE Select	ENSP00000300692.4:n.406+55_406+56insATGT
ENST00000300692.8:c.406+55_406+56insATGT	ENSP00000300692.4:n.406+55_406+56insATGT
ENST00000392884.2:c.275-226_275-225insATGT	ENSP00000376622.2:n.275-226_275-225insATGT
ENST00000526561.1:n.80-226_80-225insATGT
ENST00000529594.5:c.187+55_187+56insATGT	ENSP00000437335.1:n.187+55_187+56insATGT
ENST00000534687.5:c.288-226_288-225insATGT
NM_000732.4:c.406+55_406+56insATGT , LRG_37t1:c.406+55_406+56insATGT	NP_000723.1:n.406+55_406+56insATGT
NM_001040651.1:c.275-226_275-225insATGT	NP_001035741.1:n.275-226_275-225insATGT
NM_001040651.2:c.275-226_275-225insATGT	NP_001035741.1:n.275-226_275-225insATGT
NM_000732.6:c.406+55_406+56insATGT MANE Select	NP_000723.1:n.406+55_406+56insATGT