Canonical Allele Identifier: CA2725025503

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059135

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339727_118339728insCCAC , CM000673.2:g.118339727_118339728insCCAC	GRCh38
NC_000011.9:g.118210442_118210443insCCAC , CM000673.1:g.118210442_118210443insCCAC	GRCh37
NC_000011.8:g.117715652_117715653insCCAC	NCBI36
NG_007566.1:g.384_385insCCAC , LRG_39:g.384_385insCCAC
NG_009891.1:g.8020_8021insGGTG , LRG_37:g.8020_8021insGGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.943_944insGGTG
ENST00000695667.1:n.461_462insGGTG
ENST00000695668.1:n.2441_2442insGGTG
ENST00000300692.9:c.406+50_406+51insGGTG MANE Select	ENSP00000300692.4:n.406+50_406+51insGGTG
ENST00000300692.8:c.406+50_406+51insGGTG	ENSP00000300692.4:n.406+50_406+51insGGTG
ENST00000392884.2:c.275-231_275-230insGGTG	ENSP00000376622.2:n.275-231_275-230insGGTG
ENST00000526561.1:n.80-231_80-230insGGTG
ENST00000529594.5:c.187+50_187+51insGGTG	ENSP00000437335.1:n.187+50_187+51insGGTG
ENST00000534687.5:c.288-231_288-230insGGTG
NM_000732.4:c.406+50_406+51insGGTG , LRG_37t1:c.406+50_406+51insGGTG	NP_000723.1:n.406+50_406+51insGGTG
NM_001040651.1:c.275-231_275-230insGGTG	NP_001035741.1:n.275-231_275-230insGGTG
NM_001040651.2:c.275-231_275-230insGGTG	NP_001035741.1:n.275-231_275-230insGGTG
NM_000732.6:c.406+50_406+51insGGTG MANE Select	NP_000723.1:n.406+50_406+51insGGTG