Canonical Allele Identifier: CA400365811
Community Standard Title: NM_058216.3(RAD51C):c.1028C>G (p.Pro343Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734119C>G , CM000679.2:g.58734119C>G GRCh38
NC_000017.10:g.56811480C>G , CM000679.1:g.56811480C>G GRCh37
NC_000017.9:g.54166479C>G NCBI36
NG_023199.1:g.46518C>G , LRG_314:g.46518C>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1028C>G MANE Select NP_478123.1:p.Pro343Arg
ENST00000337432.9:c.1028C>G MANE Select ENSP00000336701.4:p.Pro343Arg
NM_058216.2:c.1028C>G NP_478123.1:p.Pro343Arg
NR_103872.1:n.932C>G
NR_103872.2:n.903C>G
ENST00000337432.8:c.1028C>G ENSP00000336701.4:p.Pro343Arg
ENST00000413590.5:c.669C>G
ENST00000461271.6:c.*1560C>G ENSP00000464056.2:n.*1560C>G
ENST00000461706.1:n.215C>G
ENST00000475762.5:c.*1664C>G ENSP00000432421.1:n.*1664C>G
ENST00000482007.5:c.*456C>G ENSP00000433332.1:n.*456C>G
ENST00000487525.5:c.*604C>G ENSP00000431637.1:n.*604C>G
ENST00000578151.1:n.241C>G
ENST00000581221.5:n.543C>G
ENST00000584804.1:c.262C>G ENSP00000463658.1:p.Leu88Val
ENST00000697680.1:c.*1992C>G ENSP00000513392.1:n.*1992C>G
ENST00000697681.1:c.*2189C>G ENSP00000513393.1:n.*2189C>G
ENST00000697683.1:c.*1964C>G ENSP00000513395.1:n.*1964C>G
ENST00000697685.1:c.*1725C>G ENSP00000513396.1:n.*1725C>G
ENST00000697686.1:c.799C>G ENSP00000513397.1:p.Leu267Val
ENST00000697689.1:c.*1442C>G ENSP00000513398.1:n.*1442C>G
ENST00000697690.1:c.906C>G ENSP00000513399.1:p.Ala302=
ENST00000697691.1:c.*1000C>G ENSP00000513400.1:n.*1000C>G
ENST00000697692.1:c.*1040C>G ENSP00000513401.1:n.*1040C>G
ENST00000697694.1:c.677C>G ENSP00000513402.1:p.Pro226Arg
ENST00000697695.1:n.1635C>G
XM_006722001.2:c.1031C>G XP_006722064.1:p.Pro344Arg
XM_006722001.4:c.1031C>G XP_006722064.1:p.Pro344Arg
XM_006722002.2:c.967C>G XP_006722065.1:p.Leu323Val
XM_006722002.4:c.967C>G XP_006722065.1:p.Leu323Val
XM_006722004.2:c.680C>G XP_006722067.1:p.Pro227Arg
XM_006722004.3:c.680C>G XP_006722067.1:p.Pro227Arg
XM_006722005.2:c.680C>G XP_006722068.1:p.Pro227Arg
XM_006722005.3:c.680C>G XP_006722068.1:p.Pro227Arg
XM_011525092.1:c.680C>G XP_011523394.1:p.Pro227Arg
XM_011525092.2:c.680C>G XP_011523394.1:p.Pro227Arg
XM_011525093.1:c.680C>G XP_011523395.1:p.Pro227Arg
XM_011525093.2:c.680C>G XP_011523395.1:p.Pro227Arg
XM_011525094.1:c.680C>G XP_011523396.1:p.Pro227Arg
XM_011525094.2:c.680C>G XP_011523396.1:p.Pro227Arg
XM_017024914.1:c.677C>G XP_016880403.1:p.Pro226Arg
XM_017024915.1:c.677C>G XP_016880404.1:p.Pro226Arg
XM_017024916.1:c.677C>G XP_016880405.1:p.Pro226Arg
XM_017024917.1:c.677C>G XP_016880406.1:p.Pro226Arg
XM_017024918.2:c.677C>G XP_016880407.1:p.Pro226Arg
XM_017024919.1:c.616C>G XP_016880408.1:p.Leu206Val
XR_934513.1:n.1246C>G
XR_934513.3:n.1677C>G
XR_934514.1:n.1249C>G
XR_934514.3:n.1680C>G
XR_934886.1:n.149+3952G>C
XR_934886.2:n.149+3952G>C