Canonical Allele Identifier: CA2616232441

Gene: CD3D

Linked Data

• gnomAD v4: 11-118339744-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339744_118339745insG , CM000673.2:g.118339744_118339745insG	GRCh38
NC_000011.9:g.118210459_118210460insG , CM000673.1:g.118210459_118210460insG	GRCh37
NC_000011.8:g.117715669_117715670insG	NCBI36
NG_007566.1:g.401_402insG , LRG_39:g.401_402insG
NG_009891.1:g.8000_8001insC , LRG_37:g.8000_8001insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.923_924insC
ENST00000695667.1:n.441_442insC
ENST00000695668.1:n.2421_2422insC
ENST00000300692.9:c.406+30_406+31insC MANE Select	ENSP00000300692.4:n.406+30_406+31insC
ENST00000300692.8:c.406+30_406+31insC	ENSP00000300692.4:n.406+30_406+31insC
ENST00000392884.2:c.275-251_275-250insC	ENSP00000376622.2:n.275-251_275-250insC
ENST00000526561.1:n.80-251_80-250insC
ENST00000529594.5:c.187+30_187+31insC	ENSP00000437335.1:n.187+30_187+31insC
ENST00000534687.5:c.288-251_288-250insC
NM_000732.4:c.406+30_406+31insC , LRG_37t1:c.406+30_406+31insC	NP_000723.1:n.406+30_406+31insC
NM_001040651.1:c.275-251_275-250insC	NP_001035741.1:n.275-251_275-250insC
NM_001040651.2:c.275-251_275-250insC	NP_001035741.1:n.275-251_275-250insC
NM_000732.6:c.406+30_406+31insC MANE Select	NP_000723.1:n.406+30_406+31insC