Canonical Allele Identifier: CA2003457102
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339945_118339960delinsTTTAAGATCAGGGAAC , CM000673.2:g.118339945_118339960delinsTTTAAGATCAGGGAAC GRCh38
NC_000011.9:g.118210660_118210675delinsTTTAAGATCAGGGAAC , CM000673.1:g.118210660_118210675delinsTTTAAGATCAGGGAAC GRCh37
NC_000011.8:g.117715870_117715885delinsTTTAAGATCAGGGAAC NCBI36
NG_007566.1:g.602_617delinsTTTAAGATCAGGGAAC , LRG_39:g.602_617delinsTTTAAGATCAGGGAAC
NG_009891.1:g.7785_7800delinsGTTCCCTGATCTTAAA , LRG_37:g.7785_7800delinsGTTCCCTGATCTTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.708_723delinsGTTCCCTGATCTTAAA
ENST00000695667.1:n.280-54_280-39delinsGTTCCCTGATCTTAAA
ENST00000695668.1:n.2260-54_2260-39delinsGTTCCCTGATCTTAAA
ENST00000300692.9:c.275-54_275-39delinsGTTCCCTGATCTTAAA MANE Select ENSP00000300692.4:n.275-54_275-39delinsGTTCCCTGATCTTAAA
ENST00000300692.8:c.275-54_275-39delinsGTTCCCTGATCTTAAA ENSP00000300692.4:n.275-54_275-39delinsGTTCCCTGATCTTAAA
ENST00000392884.2:c.274+415_274+430delinsGTTCCCTGATCTTAAA ENSP00000376622.2:n.274+415_274+430delinsGTTCCCTGATCTTAAA
ENST00000526561.1:n.80-466_80-451delinsGTTCCCTGATCTTAAA
ENST00000529594.5:c.56-54_56-39delinsGTTCCCTGATCTTAAA ENSP00000437335.1:n.56-54_56-39delinsGTTCCCTGATCTTAAA
ENST00000534687.5:c.287+415_287+430delinsGTTCCCTGATCTTAAA
NM_000732.4:c.275-54_275-39delinsGTTCCCTGATCTTAAA , LRG_37t1:c.275-54_275-39delinsGTTCCCTGATCTTAAA NP_000723.1:n.275-54_275-39delinsGTTCCCTGATCTTAAA
NM_001040651.1:c.274+415_274+430delinsGTTCCCTGATCTTAAA NP_001035741.1:n.274+415_274+430delinsGTTCCCTGATCTTAAA
NM_001040651.2:c.274+415_274+430delinsGTTCCCTGATCTTAAA NP_001035741.1:n.274+415_274+430delinsGTTCCCTGATCTTAAA
NM_000732.6:c.275-54_275-39delinsGTTCCCTGATCTTAAA MANE Select NP_000723.1:n.275-54_275-39delinsGTTCCCTGATCTTAAA