Canonical Allele Identifier: CA918978569

Gene: CD3D

Linked Data

• dbSNP Id: rs1555119652

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339743delinsCACACACAC , CM000673.2:g.118339743delinsCACACACAC	GRCh38
NC_000011.9:g.118210458delinsCACACACAC , CM000673.1:g.118210458delinsCACACACAC	GRCh37
NC_000011.8:g.117715668delinsCACACACAC	NCBI36
NG_007566.1:g.400delinsCACACACAC , LRG_39:g.400delinsCACACACAC
NG_009891.1:g.8002delinsGTGTGTGTG , LRG_37:g.8002delinsGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.925delinsGTGTGTGTG
ENST00000695667.1:n.443delinsGTGTGTGTG
ENST00000695668.1:n.2423delinsGTGTGTGTG
ENST00000300692.9:c.406+32delinsGTGTGTGTG MANE Select	ENSP00000300692.4:n.406+32delinsGTGTGTGTG
ENST00000300692.8:c.406+32delinsGTGTGTGTG	ENSP00000300692.4:n.406+32delinsGTGTGTGTG
ENST00000392884.2:c.275-249delinsGTGTGTGTG	ENSP00000376622.2:n.275-249delinsGTGTGTGTG
ENST00000526561.1:n.80-249delinsGTGTGTGTG
ENST00000529594.5:c.187+32delinsGTGTGTGTG	ENSP00000437335.1:n.187+32delinsGTGTGTGTG
ENST00000534687.5:c.288-249delinsGTGTGTGTG
NM_000732.4:c.406+32delinsGTGTGTGTG , LRG_37t1:c.406+32delinsGTGTGTGTG	NP_000723.1:n.406+32delinsGTGTGTGTG
NM_001040651.1:c.275-249delinsGTGTGTGTG	NP_001035741.1:n.275-249delinsGTGTGTGTG
NM_001040651.2:c.275-249delinsGTGTGTGTG	NP_001035741.1:n.275-249delinsGTGTGTGTG
NM_000732.6:c.406+32delinsGTGTGTGTG MANE Select	NP_000723.1:n.406+32delinsGTGTGTGTG