Canonical Allele Identifier: CA6301847
Community Standard Title: NM_000732.6(CD3D):c.457C>T (p.Arg153Ter)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339221G>A , CM000673.2:g.118339221G>A GRCh38
NC_000011.9:g.118209936G>A , CM000673.1:g.118209936G>A GRCh37
NC_000011.8:g.117715146G>A NCBI36
NG_009891.1:g.8524C>T , LRG_37:g.8524C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.457C>T MANE Select NP_000723.1:p.Arg153Ter
ENST00000300692.9:c.457C>T MANE Select ENSP00000300692.4:p.Arg153Ter
NM_000732.4:c.457C>T , LRG_37t1:c.457C>T NP_000723.1:p.Arg153Ter
NM_001040651.1:c.325C>T NP_001035741.1:p.Arg109Ter
NM_001040651.2:c.325C>T NP_001035741.1:p.Arg109Ter
ENST00000300692.8:c.457C>T ENSP00000300692.4:p.Arg153Ter
ENST00000392884.2:c.325C>T ENSP00000376622.2:p.Arg109Ter
ENST00000526561.1:n.130C>T
ENST00000529594.5:c.238C>T ENSP00000437335.1:p.Arg80Ter
ENST00000534687.5:c.338C>T
ENST00000695666.1:n.1224C>T
ENST00000695667.1:n.742C>T