Canonical Allele Identifier: CA658684026
Community Standard Title: NM_002878.4(RAD51D):c.963dup (p.Thr322HisfsTer5)
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35100978dup , CM000679.2:g.35100978dup GRCh38
NC_000017.10:g.33427997dup , CM000679.1:g.33427997dup GRCh37
NC_000017.9:g.30452110dup NCBI36
NG_031858.1:g.23893dup , LRG_516:g.23893dup

Transcript Alleles

HGVS Amino-acid Change
NM_002878.4:c.963dup MANE Select NP_002869.3:p.Thr322HisfsTer5
ENST00000345365.11:c.963dup MANE Select ENSP00000338790.6:p.Thr322HisfsTer5
NM_001142571.1:c.1023dup NP_001136043.1:p.Thr342HisfsTer5
NM_001142571.2:c.1023dup NP_001136043.1:p.Thr342HisfsTer5
NM_002878.3:c.963dup , LRG_516t1:c.963dup NP_002869.3:p.Thr322HisfsTer5
NM_133629.2:c.627dup NP_598332.1:p.Thr210HisfsTer5
NM_133629.3:c.627dup NP_598332.1:p.Thr210HisfsTer5
NR_037711.1:n.1100dup
NR_037711.2:n.989dup
NR_037712.1:n.965dup
NR_037712.2:n.854dup
NR_037714.1:n.655+224dup
ENST00000335858.11:c.627dup ENSP00000338408.6:p.Thr210HisfsTer5
ENST00000345365.10:c.963dup ENSP00000338790.6:p.Thr322HisfsTer5
ENST00000394589.8:c.963dup ENSP00000378090.4:p.Thr322HisfsTer5
ENST00000460118.6:c.432dup ENSP00000464356.2:p.Thr145HisfsTer5
ENST00000586044.5:c.*694dup ENSP00000465584.1:n.*694dup
ENST00000586186.3:c.828dup ENSP00000468273.3:p.Thr277HisfsTer5
ENST00000586210.5:c.*557dup ENSP00000465612.1:n.*557dup
ENST00000587405.6:c.606dup ENSP00000466478.2:p.Thr203HisfsTer5
ENST00000587977.5:c.*703dup ENSP00000466587.1:n.*703dup
ENST00000588372.5:c.*446dup ENSP00000468764.1:n.*446dup
ENST00000588594.5:c.*559dup ENSP00000465366.1:n.*559dup
ENST00000590016.5:c.1023dup ENSP00000466399.1:p.Thr342HisfsTer5
ENST00000590016.6:c.1023dup ENSP00000466399.1:p.Thr342HisfsTer5
ENST00000591723.5:c.372+224dup ENSP00000467986.1:n.372+224dup
ENST00000592181.1:c.546+224dup ENSP00000464799.1:n.546+224dup
ENST00000592577.6:c.606dup ENSP00000466839.2:p.Thr203HisfsTer5
ENST00000593039.5:c.426+224dup ENSP00000466834.1:n.426+224dup