Canonical Allele Identifier: CA191987
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35118564_35118579del , CM000679.2:g.35118564_35118579del GRCh38
NC_000017.10:g.33445583_33445598del , CM000679.1:g.33445583_33445598del GRCh37
NC_000017.9:g.30469696_30469711del NCBI36
NG_031858.1:g.6291_6306del , LRG_516:g.6291_6306del
NG_054719.1:g.1986_2001del

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.185_200del ENSP00000468273.3:p.Ser62LeufsTer9
ENST00000587405.6:c.-95+2712_-95+2727del ENSP00000466478.2:n.-95+2712_-95+2727del
ENST00000590016.6:c.144+532_144+547del ENSP00000466399.1:n.144+532_144+547del
ENST00000590631.2:n.436+532_436+547del
ENST00000592577.6:c.-173_-158del ENSP00000466839.2:n.-173_-158del
ENST00000345365.11:c.185_200del MANE Select ENSP00000338790.6:p.Ser62LeufsTer9
ENST00000335858.11:c.144+532_144+547del ENSP00000338408.6:n.144+532_144+547del
ENST00000345365.10:c.185_200del ENSP00000338790.6:p.Ser62LeufsTer9
ENST00000394589.8:c.185_200del ENSP00000378090.4:p.Ser62LeufsTer9
ENST00000415064.6:n.335_350del
ENST00000460118.6:c.-208+532_-208+547del ENSP00000464356.2:n.-208+532_-208+547del
ENST00000585343.5:c.88_103del
ENST00000585947.5:n.159+2712_159+2727del
ENST00000585982.5:n.239+532_239+547del
ENST00000586044.5:c.144+532_144+547del ENSP00000465584.1:n.144+532_144+547del
ENST00000586186.2:c.88_103del
ENST00000586210.5:c.185_200del ENSP00000465612.1:p.Ser62LeufsTer9
ENST00000587405.5:c.-95+2712_-95+2727del ENSP00000466478.1:n.-95+2712_-95+2727del
ENST00000587977.5:c.185_200del ENSP00000466587.1:p.Ser62LeufsTer9
ENST00000587982.5:n.191+2712_191+2727del
ENST00000588372.5:c.-95+2712_-95+2727del ENSP00000468764.1:n.-95+2712_-95+2727del
ENST00000588594.5:c.144+532_144+547del ENSP00000465366.1:n.144+532_144+547del
ENST00000589506.1:n.355+532_355+547del
ENST00000590016.5:c.144+532_144+547del ENSP00000466399.1:n.144+532_144+547del
ENST00000590631.1:c.-52+532_-52+547del ENSP00000465033.1:n.-52+532_-52+547del
ENST00000591723.5:c.-134+2712_-134+2727del ENSP00000467986.1:n.-134+2712_-134+2727del
ENST00000592181.1:c.-95+532_-95+547del ENSP00000464799.1:n.-95+532_-95+547del
ENST00000592430.5:n.232+2712_232+2727del
ENST00000592577.5:c.191_206del ENSP00000466839.1:p.Ser64LeufsTer9
ENST00000592850.5:c.88_103del
ENST00000592928.2:n.88_103del
ENST00000593039.5:c.3+2712_3+2727del ENSP00000466834.1:n.3+2712_3+2727del
NM_001142571.1:c.144+532_144+547del NP_001136043.1:n.144+532_144+547del
NM_002878.3:c.185_200del , LRG_516t1:c.185_200del NP_002869.3:p.Ser62LeufsTer9
NM_133629.2:c.144+532_144+547del NP_598332.1:n.144+532_144+547del
NR_037711.1:n.400+532_400+547del
NR_037712.1:n.400+532_400+547del
NR_037714.1:n.232+2712_232+2727del
NM_001142571.2:c.144+532_144+547del NP_001136043.1:n.144+532_144+547del
NM_133629.3:c.144+532_144+547del NP_598332.1:n.144+532_144+547del
NR_037711.2:n.289+532_289+547del
NR_037712.2:n.289+532_289+547del
NM_002878.4:c.185_200del MANE Select NP_002869.3:p.Ser62LeufsTer9