Canonical Allele Identifier: CA400366053
Community Standard Title: NM_058216.3(RAD51C):c.1051G>T (p.Val351Phe)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734142G>T , CM000679.2:g.58734142G>T GRCh38
NC_000017.10:g.56811503G>T , CM000679.1:g.56811503G>T GRCh37
NC_000017.9:g.54166502G>T NCBI36
NG_023199.1:g.46541G>T , LRG_314:g.46541G>T

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1051G>T MANE Select NP_478123.1:p.Val351Phe
ENST00000337432.9:c.1051G>T MANE Select ENSP00000336701.4:p.Val351Phe
NM_058216.2:c.1051G>T NP_478123.1:p.Val351Phe
NR_103872.1:n.955G>T
NR_103872.2:n.926G>T
ENST00000337432.8:c.1051G>T ENSP00000336701.4:p.Val351Phe
ENST00000413590.5:c.692G>T
ENST00000461271.6:c.*1583G>T ENSP00000464056.2:n.*1583G>T
ENST00000461706.1:n.238G>T
ENST00000475762.5:c.*1687G>T ENSP00000432421.1:n.*1687G>T
ENST00000482007.5:c.*479G>T ENSP00000433332.1:n.*479G>T
ENST00000487525.5:c.*627G>T ENSP00000431637.1:n.*627G>T
ENST00000578151.1:n.264G>T
ENST00000581221.5:n.566G>T
ENST00000584804.1:c.285G>T ENSP00000463658.1:p.Leu95Phe
ENST00000697680.1:c.*2015G>T ENSP00000513392.1:n.*2015G>T
ENST00000697681.1:c.*2212G>T ENSP00000513393.1:n.*2212G>T
ENST00000697683.1:c.*1987G>T ENSP00000513395.1:n.*1987G>T
ENST00000697685.1:c.*1748G>T ENSP00000513396.1:n.*1748G>T
ENST00000697686.1:c.822G>T ENSP00000513397.1:p.Leu274Phe
ENST00000697689.1:c.*1465G>T ENSP00000513398.1:n.*1465G>T
ENST00000697690.1:c.*11G>T ENSP00000513399.1:n.*11G>T
ENST00000697691.1:c.*1023G>T ENSP00000513400.1:n.*1023G>T
ENST00000697692.1:c.*1063G>T ENSP00000513401.1:n.*1063G>T
ENST00000697694.1:c.700G>T ENSP00000513402.1:p.Val234Phe
ENST00000697695.1:n.1658G>T
XM_006722001.2:c.1054G>T XP_006722064.1:p.Val352Phe
XM_006722001.4:c.1054G>T XP_006722064.1:p.Val352Phe
XM_006722002.2:c.990G>T XP_006722065.1:p.Leu330Phe
XM_006722002.4:c.990G>T XP_006722065.1:p.Leu330Phe
XM_006722004.2:c.703G>T XP_006722067.1:p.Val235Phe
XM_006722004.3:c.703G>T XP_006722067.1:p.Val235Phe
XM_006722005.2:c.703G>T XP_006722068.1:p.Val235Phe
XM_006722005.3:c.703G>T XP_006722068.1:p.Val235Phe
XM_011525092.1:c.703G>T XP_011523394.1:p.Val235Phe
XM_011525092.2:c.703G>T XP_011523394.1:p.Val235Phe
XM_011525093.1:c.703G>T XP_011523395.1:p.Val235Phe
XM_011525093.2:c.703G>T XP_011523395.1:p.Val235Phe
XM_011525094.1:c.703G>T XP_011523396.1:p.Val235Phe
XM_011525094.2:c.703G>T XP_011523396.1:p.Val235Phe
XM_017024914.1:c.700G>T XP_016880403.1:p.Val234Phe
XM_017024915.1:c.700G>T XP_016880404.1:p.Val234Phe
XM_017024916.1:c.700G>T XP_016880405.1:p.Val234Phe
XM_017024917.1:c.700G>T XP_016880406.1:p.Val234Phe
XM_017024918.2:c.700G>T XP_016880407.1:p.Val234Phe
XM_017024919.1:c.639G>T XP_016880408.1:p.Leu213Phe
XR_934513.1:n.1269G>T
XR_934513.3:n.1700G>T
XR_934514.1:n.1272G>T
XR_934514.3:n.1703G>T
XR_934886.1:n.149+3929C>A
XR_934886.2:n.149+3929C>A