Canonical Allele Identifier: CA2725025484

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059097

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339717_118339718insTCAC , CM000673.2:g.118339717_118339718insTCAC	GRCh38
NC_000011.9:g.118210432_118210433insTCAC , CM000673.1:g.118210432_118210433insTCAC	GRCh37
NC_000011.8:g.117715642_117715643insTCAC	NCBI36
NG_007566.1:g.374_375insTCAC , LRG_39:g.374_375insTCAC
NG_009891.1:g.8030_8031insAGTG , LRG_37:g.8030_8031insAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.953_954insAGTG
ENST00000695667.1:n.471_472insAGTG
ENST00000300692.9:c.406+60_406+61insAGTG MANE Select	ENSP00000300692.4:n.406+60_406+61insAGTG
ENST00000300692.8:c.406+60_406+61insAGTG	ENSP00000300692.4:n.406+60_406+61insAGTG
ENST00000392884.2:c.275-221_275-220insAGTG	ENSP00000376622.2:n.275-221_275-220insAGTG
ENST00000526561.1:n.80-221_80-220insAGTG
ENST00000529594.5:c.187+60_187+61insAGTG	ENSP00000437335.1:n.187+60_187+61insAGTG
ENST00000534687.5:c.288-221_288-220insAGTG
NM_000732.4:c.406+60_406+61insAGTG , LRG_37t1:c.406+60_406+61insAGTG	NP_000723.1:n.406+60_406+61insAGTG
NM_001040651.1:c.275-221_275-220insAGTG	NP_001035741.1:n.275-221_275-220insAGTG
NM_001040651.2:c.275-221_275-220insAGTG	NP_001035741.1:n.275-221_275-220insAGTG
NM_000732.6:c.406+60_406+61insAGTG MANE Select	NP_000723.1:n.406+60_406+61insAGTG