Canonical Allele Identifier: CA2003456950

Gene: CD3D

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339709_118339725delinsTACACACACACACACAC , CM000673.2:g.118339709_118339725delinsTACACACACACACACAC	GRCh38
NC_000011.9:g.118210424_118210440delinsTACACACACACACACAC , CM000673.1:g.118210424_118210440delinsTACACACACACACACAC	GRCh37
NC_000011.8:g.117715634_117715650delinsTACACACACACACACAC	NCBI36
NG_007566.1:g.366_382delinsTACACACACACACACAC , LRG_39:g.366_382delinsTACACACACACACACAC
NG_009891.1:g.8020_8036delinsGTGTGTGTGTGTGTGTA , LRG_37:g.8020_8036delinsGTGTGTGTGTGTGTGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.943_959delinsGTGTGTGTGTGTGTGTA
ENST00000695667.1:n.461_477delinsGTGTGTGTGTGTGTGTA
ENST00000300692.9:c.406+50_406+66delinsGTGTGTGTGTGTGTGTA MANE Select	ENSP00000300692.4:n.406+50_406+66delinsGTGTGTGTGTGTGTGTA
ENST00000300692.8:c.406+50_406+66delinsGTGTGTGTGTGTGTGTA	ENSP00000300692.4:n.406+50_406+66delinsGTGTGTGTGTGTGTGTA
ENST00000392884.2:c.275-231_275-215delinsGTGTGTGTGTGTGTGTA	ENSP00000376622.2:n.275-231_275-215delinsGTGTGTGTGTGTGTGTA
ENST00000526561.1:n.80-231_80-215delinsGTGTGTGTGTGTGTGTA
ENST00000529594.5:c.187+50_187+66delinsGTGTGTGTGTGTGTGTA	ENSP00000437335.1:n.187+50_187+66delinsGTGTGTGTGTGTGTGTA
ENST00000534687.5:c.288-231_288-215delinsGTGTGTGTGTGTGTGTA
NM_000732.4:c.406+50_406+66delinsGTGTGTGTGTGTGTGTA , LRG_37t1:c.406+50_406+66delinsGTGTGTGTGTGTGTGTA	NP_000723.1:n.406+50_406+66delinsGTGTGTGTGTGTGTGTA
NM_001040651.1:c.275-231_275-215delinsGTGTGTGTGTGTGTGTA	NP_001035741.1:n.275-231_275-215delinsGTGTGTGTGTGTGTGTA
NM_001040651.2:c.275-231_275-215delinsGTGTGTGTGTGTGTGTA	NP_001035741.1:n.275-231_275-215delinsGTGTGTGTGTGTGTGTA
NM_000732.6:c.406+50_406+66delinsGTGTGTGTGTGTGTGTA MANE Select	NP_000723.1:n.406+50_406+66delinsGTGTGTGTGTGTGTGTA