Canonical Allele Identifier: CA192851
Gene: RAD51D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35107381dup , CM000679.2:g.35107381dup GRCh38
NC_000017.10:g.33434400dup , CM000679.1:g.33434400dup GRCh37
NC_000017.9:g.30458513dup NCBI36
NG_031858.1:g.17489dup , LRG_516:g.17489dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.330dup ENSP00000468273.3:p.Ser111Ter
ENST00000587405.6:c.-28dup ENSP00000466478.2:n.-28dup
ENST00000590016.6:c.390dup ENSP00000466399.1:p.Ser131Ter
ENST00000590631.2:n.437-900dup
ENST00000592577.6:c.-28dup ENSP00000466839.2:n.-28dup
ENST00000345365.11:c.330dup MANE Select ENSP00000338790.6:p.Ser111Ter
ENST00000335858.11:c.145-900dup ENSP00000338408.6:n.145-900dup
ENST00000345365.10:c.330dup ENSP00000338790.6:p.Ser111Ter
ENST00000394589.8:c.330dup ENSP00000378090.4:p.Ser111Ter
ENST00000415064.6:n.480dup
ENST00000460118.6:c.-141dup ENSP00000464356.2:n.-141dup
ENST00000585343.5:c.412dup
ENST00000585947.5:n.226dup
ENST00000585982.5:n.485dup
ENST00000586044.5:c.*61dup ENSP00000465584.1:n.*61dup
ENST00000586186.2:c.233dup
ENST00000586210.5:c.264-259dup ENSP00000465612.1:n.264-259dup
ENST00000587405.5:c.-28dup ENSP00000466478.1:n.-28dup
ENST00000587977.5:c.*86-259dup ENSP00000466587.1:n.*86-259dup
ENST00000587982.5:n.258dup
ENST00000588372.5:c.-28dup ENSP00000468764.1:n.-28dup
ENST00000588594.5:c.*61dup ENSP00000465366.1:n.*61dup
ENST00000589506.1:n.422dup
ENST00000590016.5:c.390dup ENSP00000466399.1:p.Ser131Ter
ENST00000590631.1:c.-51-900dup ENSP00000465033.1:n.-51-900dup
ENST00000591723.5:c.-67dup ENSP00000467986.1:n.-67dup
ENST00000592181.1:c.-28dup ENSP00000464799.1:n.-28dup
ENST00000592430.5:n.299dup
ENST00000592577.5:c.336dup ENSP00000466839.1:p.Ser113Ter
ENST00000592850.5:c.346-900dup
ENST00000592928.2:n.167-900dup
ENST00000593039.5:c.4-900dup ENSP00000466834.1:n.4-900dup
NM_001142571.1:c.390dup NP_001136043.1:p.Ser131Ter
NM_002878.3:c.330dup , LRG_516t1:c.330dup NP_002869.3:p.Ser111Ter
NM_133629.2:c.145-900dup NP_598332.1:n.145-900dup
NR_037711.1:n.467dup
NR_037712.1:n.467dup
NR_037714.1:n.233-900dup
NM_001142571.2:c.390dup NP_001136043.1:p.Ser131Ter
NM_133629.3:c.145-900dup NP_598332.1:n.145-900dup
NR_037711.2:n.356dup
NR_037712.2:n.356dup
NM_002878.4:c.330dup MANE Select NP_002869.3:p.Ser111Ter