Canonical Allele Identifier: CA2257361546
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35106398A= , CM000679.2:g.35106398A= GRCh38
NC_000017.10:g.33433417A= , CM000679.1:g.33433417A= GRCh37
NC_000017.9:g.30457530A= NCBI36
NG_031858.1:g.18472T= , LRG_516:g.18472T=

Transcript Alleles

HGVS Amino-acid Change
NM_002878.4:c.564T= MANE Select NP_002869.3:p.Thr188=
ENST00000345365.11:c.564T= MANE Select ENSP00000338790.6:p.Thr188=
NM_001142571.1:c.624T= NP_001136043.1:p.Thr208=
NM_001142571.2:c.624T= NP_001136043.1:p.Thr208=
NM_002878.3:c.564T= , LRG_516t1:c.564T= NP_002869.3:p.Thr188=
NM_133629.2:c.228T= NP_598332.1:p.Thr76=
NM_133629.3:c.228T= NP_598332.1:p.Thr76=
NR_037711.1:n.701T=
NR_037711.2:n.590T=
NR_037712.1:n.566T=
NR_037712.2:n.455T=
NR_037714.1:n.316T=
ENST00000335858.11:c.228T= ENSP00000338408.6:p.Thr76=
ENST00000345365.10:c.564T= ENSP00000338790.6:p.Thr188=
ENST00000394589.8:c.564T= ENSP00000378090.4:p.Thr188=
ENST00000415064.6:n.714T=
ENST00000460118.6:c.33T= ENSP00000464356.2:p.Thr11=
ENST00000585947.5:n.460T=
ENST00000585982.5:n.584T=
ENST00000586044.5:c.*295T= ENSP00000465584.1:n.*295T=
ENST00000586186.3:c.429T= ENSP00000468273.3:p.Thr143=
ENST00000586210.5:c.*158T= ENSP00000465612.1:n.*158T=
ENST00000587405.5:c.207T= ENSP00000466478.1:p.Thr69=
ENST00000587405.6:c.207T= ENSP00000466478.2:p.Thr69=
ENST00000587977.5:c.*304T= ENSP00000466587.1:n.*304T=
ENST00000587982.5:n.357T=
ENST00000588372.5:c.207T= ENSP00000468764.1:p.Thr69=
ENST00000588594.5:c.*160T= ENSP00000465366.1:n.*160T=
ENST00000590016.5:c.624T= ENSP00000466399.1:p.Thr208=
ENST00000590016.6:c.624T= ENSP00000466399.1:p.Thr208=
ENST00000590631.1:c.33T= ENSP00000465033.1:p.Thr11=
ENST00000590631.2:n.520T=
ENST00000591723.5:c.33T= ENSP00000467986.1:p.Thr11=
ENST00000592181.1:c.207T= ENSP00000464799.1:p.Thr69=
ENST00000592430.5:n.533T=
ENST00000592577.5:c.570T= ENSP00000466839.1:p.Thr190=
ENST00000592577.6:c.207T= ENSP00000466839.2:p.Thr69=
ENST00000593039.5:c.87T= ENSP00000466834.1:p.Thr29=