Canonical Allele Identifier: CA2257361229
Gene: RAD51D HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35105653A>G , CM000679.2:g.35105653A>G GRCh38
NC_000017.10:g.33432672A>G , CM000679.1:g.33432672A>G GRCh37
NC_000017.9:g.30456785A>G NCBI36
NG_031858.1:g.19217T>C , LRG_516:g.19217T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000586186.3:c.441+733T>C ENSP00000468273.3:n.441+733T>C
ENST00000587405.6:c.219+733T>C ENSP00000466478.2:n.219+733T>C
ENST00000590016.6:c.636+733T>C ENSP00000466399.1:n.636+733T>C
ENST00000590631.2:n.532+733T>C
ENST00000592577.6:c.219+733T>C ENSP00000466839.2:n.219+733T>C
ENST00000345365.11:c.576+733T>C MANE Select ENSP00000338790.6:n.576+733T>C
ENST00000335858.11:c.240+733T>C ENSP00000338408.6:n.240+733T>C
ENST00000345365.10:c.576+733T>C ENSP00000338790.6:n.576+733T>C
ENST00000394589.8:c.576+733T>C ENSP00000378090.4:n.576+733T>C
ENST00000415064.6:n.848+475T>C
ENST00000460118.6:c.45+733T>C ENSP00000464356.2:n.45+733T>C
ENST00000586044.5:c.*307+733T>C ENSP00000465584.1:n.*307+733T>C
ENST00000586210.5:c.*170+733T>C ENSP00000465612.1:n.*170+733T>C
ENST00000587405.5:c.219+733T>C ENSP00000466478.1:n.219+733T>C
ENST00000587977.5:c.*316+733T>C ENSP00000466587.1:n.*316+733T>C
ENST00000587982.5:n.627+475T>C
ENST00000588372.5:c.*59+475T>C ENSP00000468764.1:n.*59+475T>C
ENST00000588594.5:c.*172+733T>C ENSP00000465366.1:n.*172+733T>C
ENST00000590016.5:c.636+733T>C ENSP00000466399.1:n.636+733T>C
ENST00000590631.1:c.45+733T>C ENSP00000465033.1:n.45+733T>C
ENST00000591723.5:c.45+733T>C ENSP00000467986.1:n.45+733T>C
ENST00000592181.1:c.219+733T>C ENSP00000464799.1:n.219+733T>C
ENST00000592577.5:c.582+733T>C ENSP00000466839.1:n.582+733T>C
ENST00000593039.5:c.99+733T>C ENSP00000466834.1:n.99+733T>C
NM_001142571.1:c.636+733T>C NP_001136043.1:n.636+733T>C
NM_002878.3:c.576+733T>C , LRG_516t1:c.576+733T>C NP_002869.3:n.576+733T>C
NM_133629.2:c.240+733T>C NP_598332.1:n.240+733T>C
NR_037711.1:n.713+733T>C
NR_037712.1:n.578+733T>C
NR_037714.1:n.328+733T>C
NM_001142571.2:c.636+733T>C NP_001136043.1:n.636+733T>C
NM_133629.3:c.240+733T>C NP_598332.1:n.240+733T>C
NR_037711.2:n.602+733T>C
NR_037712.2:n.467+733T>C
NM_002878.4:c.576+733T>C MANE Select NP_002869.3:n.576+733T>C
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