Canonical Allele Identifier: CA2574994329
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339974del , CM000673.2:g.118339974del GRCh38
NC_000011.9:g.118210689del , CM000673.1:g.118210689del GRCh37
NC_000011.8:g.117715899del NCBI36
NG_007566.1:g.631del , LRG_39:g.631del
NG_009891.1:g.7772del , LRG_37:g.7772del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695666.1:n.695del
ENST00000695667.1:n.280-67del
ENST00000695668.1:n.2260-67del
ENST00000300692.9:c.275-67del MANE Select ENSP00000300692.4:n.275-67del
ENST00000300692.8:c.275-67del ENSP00000300692.4:n.275-67del
ENST00000392884.2:c.274+402del ENSP00000376622.2:n.274+402del
ENST00000526561.1:n.80-479del
ENST00000529594.5:c.56-67del ENSP00000437335.1:n.56-67del
ENST00000534687.5:c.287+402del
NM_000732.4:c.275-67del , LRG_37t1:c.275-67del NP_000723.1:n.275-67del
NM_001040651.1:c.274+402del NP_001035741.1:n.274+402del
NM_001040651.2:c.274+402del NP_001035741.1:n.274+402del
NM_000732.6:c.275-67del MANE Select NP_000723.1:n.275-67del