Canonical Allele Identifier: CA6301844
Community Standard Title: NM_000732.6(CD3D):c.463C>T (p.Arg155Ter)
Gene: CD3D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118339215G>A , CM000673.2:g.118339215G>A GRCh38
NC_000011.9:g.118209930G>A , CM000673.1:g.118209930G>A GRCh37
NC_000011.8:g.117715140G>A NCBI36
NG_009891.1:g.8530C>T , LRG_37:g.8530C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000732.6:c.463C>T MANE Select NP_000723.1:p.Arg155Ter
ENST00000300692.9:c.463C>T MANE Select ENSP00000300692.4:p.Arg155Ter
NM_000732.4:c.463C>T , LRG_37t1:c.463C>T NP_000723.1:p.Arg155Ter
NM_001040651.1:c.331C>T NP_001035741.1:p.Arg111Ter
NM_001040651.2:c.331C>T NP_001035741.1:p.Arg111Ter
ENST00000300692.8:c.463C>T ENSP00000300692.4:p.Arg155Ter
ENST00000392884.2:c.331C>T ENSP00000376622.2:p.Arg111Ter
ENST00000526561.1:n.136C>T
ENST00000529594.5:c.244C>T ENSP00000437335.1:p.Arg82Ter
ENST00000534687.5:c.344C>T
ENST00000695666.1:n.1230C>T
ENST00000695667.1:n.748C>T