Canonical Allele Identifier: CA2003456955

Gene: CD3D

Linked Data

• dbSNP Id: rs1948281770

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339710_118339711insTACACACA , CM000673.2:g.118339710_118339711insTACACACA	GRCh38
NC_000011.9:g.118210425_118210426insTACACACA , CM000673.1:g.118210425_118210426insTACACACA	GRCh37
NC_000011.8:g.117715635_117715636insTACACACA	NCBI36
NG_007566.1:g.367_368insTACACACA , LRG_39:g.367_368insTACACACA
NG_009891.1:g.8035_8036insGTGTGTAT , LRG_37:g.8035_8036insGTGTGTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.958_959insGTGTGTAT
ENST00000695667.1:n.476_477insGTGTGTAT
ENST00000300692.9:c.406+65_406+66insGTGTGTAT MANE Select	ENSP00000300692.4:n.406+65_406+66insGTGTGTAT
ENST00000300692.8:c.406+65_406+66insGTGTGTAT	ENSP00000300692.4:n.406+65_406+66insGTGTGTAT
ENST00000392884.2:c.275-216_275-215insGTGTGTAT	ENSP00000376622.2:n.275-216_275-215insGTGTGTAT
ENST00000526561.1:n.80-216_80-215insGTGTGTAT
ENST00000529594.5:c.187+65_187+66insGTGTGTAT	ENSP00000437335.1:n.187+65_187+66insGTGTGTAT
ENST00000534687.5:c.288-216_288-215insGTGTGTAT
NM_000732.4:c.406+65_406+66insGTGTGTAT , LRG_37t1:c.406+65_406+66insGTGTGTAT	NP_000723.1:n.406+65_406+66insGTGTGTAT
NM_001040651.1:c.275-216_275-215insGTGTGTAT	NP_001035741.1:n.275-216_275-215insGTGTGTAT
NM_001040651.2:c.275-216_275-215insGTGTGTAT	NP_001035741.1:n.275-216_275-215insGTGTGTAT
NM_000732.6:c.406+65_406+66insGTGTGTAT MANE Select	NP_000723.1:n.406+65_406+66insGTGTGTAT