Canonical Allele Identifier: CA2257361860
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35107043G= , CM000679.2:g.35107043G= GRCh38
NC_000017.10:g.33434062G= , CM000679.1:g.33434062G= GRCh37
NC_000017.9:g.30458175G= NCBI36
NG_031858.1:g.17827C= , LRG_516:g.17827C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.345+323C= ENSP00000468273.3:n.345+323C=
ENST00000587405.6:c.68C= ENSP00000466478.2:p.Thr23=
ENST00000590016.6:c.485C= ENSP00000466399.1:p.Thr162=
ENST00000590631.2:n.437-562C=
ENST00000592577.6:c.68C= ENSP00000466839.2:p.Thr23=
ENST00000345365.11:c.425C= MANE Select ENSP00000338790.6:p.Thr142=
ENST00000335858.11:c.145-562C= ENSP00000338408.6:n.145-562C=
ENST00000345365.10:c.425C= ENSP00000338790.6:p.Thr142=
ENST00000394589.8:c.425C= ENSP00000378090.4:p.Thr142=
ENST00000415064.6:n.575C=
ENST00000460118.6:c.-107C= ENSP00000464356.2:n.-107C=
ENST00000585343.5:c.507C=
ENST00000585947.5:n.321C=
ENST00000585982.5:n.500+323C=
ENST00000586044.5:c.*156C= ENSP00000465584.1:n.*156C=
ENST00000586186.2:c.248+323C=
ENST00000586210.5:c.*19C= ENSP00000465612.1:n.*19C=
ENST00000587405.5:c.68C= ENSP00000466478.1:p.Thr23=
ENST00000587977.5:c.*165C= ENSP00000466587.1:n.*165C=
ENST00000587982.5:n.273+323C=
ENST00000588372.5:c.68C= ENSP00000468764.1:p.Thr23=
ENST00000588594.5:c.*76+323C= ENSP00000465366.1:n.*76+323C=
ENST00000590016.5:c.485C= ENSP00000466399.1:p.Thr162=
ENST00000590631.1:c.-51-562C= ENSP00000465033.1:n.-51-562C=
ENST00000591723.5:c.-52+323C= ENSP00000467986.1:n.-52+323C=
ENST00000592181.1:c.68C= ENSP00000464799.1:p.Thr23=
ENST00000592430.5:n.394C=
ENST00000592577.5:c.431C= ENSP00000466839.1:p.Thr144=
ENST00000592850.5:c.346-562C=
ENST00000592928.2:n.167-562C=
ENST00000593039.5:c.4-562C= ENSP00000466834.1:n.4-562C=
NM_001142571.1:c.485C= NP_001136043.1:p.Thr162=
NM_002878.3:c.425C= , LRG_516t1:c.425C= NP_002869.3:p.Thr142=
NM_133629.2:c.145-562C= NP_598332.1:n.145-562C=
NR_037711.1:n.562C=
NR_037712.1:n.482+323C=
NR_037714.1:n.233-562C=
NM_001142571.2:c.485C= NP_001136043.1:p.Thr162=
NM_133629.3:c.145-562C= NP_598332.1:n.145-562C=
NR_037711.2:n.451C=
NR_037712.2:n.371+323C=
NM_002878.4:c.425C= MANE Select NP_002869.3:p.Thr142=