Canonical Allele Identifier: CA2725026577

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059155

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339733_118339734insTCAC , CM000673.2:g.118339733_118339734insTCAC	GRCh38
NC_000011.9:g.118210448_118210449insTCAC , CM000673.1:g.118210448_118210449insTCAC	GRCh37
NC_000011.8:g.117715658_117715659insTCAC	NCBI36
NG_007566.1:g.390_391insTCAC , LRG_39:g.390_391insTCAC
NG_009891.1:g.8014_8015insAGTG , LRG_37:g.8014_8015insAGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.937_938insAGTG
ENST00000695667.1:n.455_456insAGTG
ENST00000695668.1:n.2435_2436insAGTG
ENST00000300692.9:c.406+44_406+45insAGTG MANE Select	ENSP00000300692.4:n.406+44_406+45insAGTG
ENST00000300692.8:c.406+44_406+45insAGTG	ENSP00000300692.4:n.406+44_406+45insAGTG
ENST00000392884.2:c.275-237_275-236insAGTG	ENSP00000376622.2:n.275-237_275-236insAGTG
ENST00000526561.1:n.80-237_80-236insAGTG
ENST00000529594.5:c.187+44_187+45insAGTG	ENSP00000437335.1:n.187+44_187+45insAGTG
ENST00000534687.5:c.288-237_288-236insAGTG
NM_000732.4:c.406+44_406+45insAGTG , LRG_37t1:c.406+44_406+45insAGTG	NP_000723.1:n.406+44_406+45insAGTG
NM_001040651.1:c.275-237_275-236insAGTG	NP_001035741.1:n.275-237_275-236insAGTG
NM_001040651.2:c.275-237_275-236insAGTG	NP_001035741.1:n.275-237_275-236insAGTG
NM_000732.6:c.406+44_406+45insAGTG MANE Select	NP_000723.1:n.406+44_406+45insAGTG