Canonical Allele Identifier: CA2725025488

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059120

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339721_118339722insCCAC , CM000673.2:g.118339721_118339722insCCAC	GRCh38
NC_000011.9:g.118210436_118210437insCCAC , CM000673.1:g.118210436_118210437insCCAC	GRCh37
NC_000011.8:g.117715646_117715647insCCAC	NCBI36
NG_007566.1:g.378_379insCCAC , LRG_39:g.378_379insCCAC
NG_009891.1:g.8026_8027insGGTG , LRG_37:g.8026_8027insGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.949_950insGGTG
ENST00000695667.1:n.467_468insGGTG
ENST00000300692.9:c.406+56_406+57insGGTG MANE Select	ENSP00000300692.4:n.406+56_406+57insGGTG
ENST00000300692.8:c.406+56_406+57insGGTG	ENSP00000300692.4:n.406+56_406+57insGGTG
ENST00000392884.2:c.275-225_275-224insGGTG	ENSP00000376622.2:n.275-225_275-224insGGTG
ENST00000526561.1:n.80-225_80-224insGGTG
ENST00000529594.5:c.187+56_187+57insGGTG	ENSP00000437335.1:n.187+56_187+57insGGTG
ENST00000534687.5:c.288-225_288-224insGGTG
NM_000732.4:c.406+56_406+57insGGTG , LRG_37t1:c.406+56_406+57insGGTG	NP_000723.1:n.406+56_406+57insGGTG
NM_001040651.1:c.275-225_275-224insGGTG	NP_001035741.1:n.275-225_275-224insGGTG
NM_001040651.2:c.275-225_275-224insGGTG	NP_001035741.1:n.275-225_275-224insGGTG
NM_000732.6:c.406+56_406+57insGGTG MANE Select	NP_000723.1:n.406+56_406+57insGGTG