Canonical Allele Identifier: CA918978571

Gene: CD3D

Linked Data

• dbSNP Id: rs1555119652

Genomic Alleles

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

Transcript Alleles

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