Canonical Allele Identifier: CA2725025485

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059106

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339719_118339720insCCACAC , CM000673.2:g.118339719_118339720insCCACAC	GRCh38
NC_000011.9:g.118210434_118210435insCCACAC , CM000673.1:g.118210434_118210435insCCACAC	GRCh37
NC_000011.8:g.117715644_117715645insCCACAC	NCBI36
NG_007566.1:g.376_377insCCACAC , LRG_39:g.376_377insCCACAC
NG_009891.1:g.8030_8031insGGTGTG , LRG_37:g.8030_8031insGGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.953_954insGGTGTG
ENST00000695667.1:n.471_472insGGTGTG
ENST00000300692.9:c.406+60_406+61insGGTGTG MANE Select	ENSP00000300692.4:n.406+60_406+61insGGTGTG
ENST00000300692.8:c.406+60_406+61insGGTGTG	ENSP00000300692.4:n.406+60_406+61insGGTGTG
ENST00000392884.2:c.275-221_275-220insGGTGTG	ENSP00000376622.2:n.275-221_275-220insGGTGTG
ENST00000526561.1:n.80-221_80-220insGGTGTG
ENST00000529594.5:c.187+60_187+61insGGTGTG	ENSP00000437335.1:n.187+60_187+61insGGTGTG
ENST00000534687.5:c.288-221_288-220insGGTGTG
NM_000732.4:c.406+60_406+61insGGTGTG , LRG_37t1:c.406+60_406+61insGGTGTG	NP_000723.1:n.406+60_406+61insGGTGTG
NM_001040651.1:c.275-221_275-220insGGTGTG	NP_001035741.1:n.275-221_275-220insGGTGTG
NM_001040651.2:c.275-221_275-220insGGTGTG	NP_001035741.1:n.275-221_275-220insGGTGTG
NM_000732.6:c.406+60_406+61insGGTGTG MANE Select	NP_000723.1:n.406+60_406+61insGGTGTG