Canonical Allele Identifier: CA400365036
Community Standard Title: NM_058216.3(RAD51C):c.1000G>C (p.Glu334Gln)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732518G>C , CM000679.2:g.58732518G>C GRCh38
NC_000017.10:g.56809879G>C , CM000679.1:g.56809879G>C GRCh37
NC_000017.9:g.54164878G>C NCBI36
NG_023199.1:g.44917G>C , LRG_314:g.44917G>C

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1000G>C MANE Select NP_478123.1:p.Glu334Gln
ENST00000337432.9:c.1000G>C MANE Select ENSP00000336701.4:p.Glu334Gln
NM_058216.2:c.1000G>C NP_478123.1:p.Glu334Gln
NR_103872.1:n.904G>C
NR_103872.2:n.875G>C
ENST00000337432.8:c.1000G>C ENSP00000336701.4:p.Glu334Gln
ENST00000413590.5:c.641G>C
ENST00000461271.6:c.649G>C ENSP00000464056.2:p.Glu217Gln
ENST00000461706.1:n.187G>C
ENST00000475762.5:c.*1636G>C ENSP00000432421.1:n.*1636G>C
ENST00000482007.5:c.*428G>C ENSP00000433332.1:n.*428G>C
ENST00000487525.5:c.*576G>C ENSP00000431637.1:n.*576G>C
ENST00000578151.1:n.240-1600G>C
ENST00000581221.5:n.515G>C
ENST00000583539.5:c.1000G>C ENSP00000463121.1:p.Glu334Gln
ENST00000584617.5:c.722G>C
ENST00000584804.1:c.234G>C ENSP00000463658.1:p.Arg78Ser
ENST00000697680.1:c.*1964G>C ENSP00000513392.1:n.*1964G>C
ENST00000697681.1:c.*2161G>C ENSP00000513393.1:n.*2161G>C
ENST00000697683.1:c.*1936G>C ENSP00000513395.1:n.*1936G>C
ENST00000697685.1:c.*1697G>C ENSP00000513396.1:n.*1697G>C
ENST00000697686.1:c.771G>C ENSP00000513397.1:p.Arg257Ser
ENST00000697689.1:c.*1441-1600G>C ENSP00000513398.1:n.*1441-1600G>C
ENST00000697690.1:c.905-1600G>C ENSP00000513399.1:n.905-1600G>C
ENST00000697691.1:c.*972G>C ENSP00000513400.1:n.*972G>C
ENST00000697692.1:c.*1012G>C ENSP00000513401.1:n.*1012G>C
ENST00000697694.1:c.649G>C ENSP00000513402.1:p.Glu217Gln
ENST00000697695.1:n.1607G>C
XM_006722001.2:c.1003G>C XP_006722064.1:p.Glu335Gln
XM_006722001.4:c.1003G>C XP_006722064.1:p.Glu335Gln
XM_006722002.2:c.939G>C XP_006722065.1:p.Arg313Ser
XM_006722002.4:c.939G>C XP_006722065.1:p.Arg313Ser
XM_006722004.2:c.652G>C XP_006722067.1:p.Glu218Gln
XM_006722004.3:c.652G>C XP_006722067.1:p.Glu218Gln
XM_006722005.2:c.652G>C XP_006722068.1:p.Glu218Gln
XM_006722005.3:c.652G>C XP_006722068.1:p.Glu218Gln
XM_011525092.1:c.652G>C XP_011523394.1:p.Glu218Gln
XM_011525092.2:c.652G>C XP_011523394.1:p.Glu218Gln
XM_011525093.1:c.652G>C XP_011523395.1:p.Glu218Gln
XM_011525093.2:c.652G>C XP_011523395.1:p.Glu218Gln
XM_011525094.1:c.652G>C XP_011523396.1:p.Glu218Gln
XM_011525094.2:c.652G>C XP_011523396.1:p.Glu218Gln
XM_017024914.1:c.649G>C XP_016880403.1:p.Glu217Gln
XM_017024915.1:c.649G>C XP_016880404.1:p.Glu217Gln
XM_017024916.1:c.649G>C XP_016880405.1:p.Glu217Gln
XM_017024917.1:c.649G>C XP_016880406.1:p.Glu217Gln
XM_017024918.2:c.649G>C XP_016880407.1:p.Glu217Gln
XM_017024919.1:c.588G>C XP_016880408.1:p.Arg196Ser
XR_934513.1:n.1218G>C
XR_934513.3:n.1649G>C
XR_934514.1:n.1221G>C
XR_934514.3:n.1652G>C
XR_934886.1:n.149+5553C>G
XR_934886.2:n.149+5553C>G