Canonical Allele Identifier: CA400354469

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709983G>C , CM000679.2:g.58709983G>C	GRCh38
NC_000017.10:g.56787344G>C , CM000679.1:g.56787344G>C	GRCh37
NC_000017.9:g.54142343G>C	NCBI36
NG_023199.1:g.22382G>C , LRG_314:g.22382G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.830G>C MANE Select	NP_478123.1:p.Arg277Thr
ENST00000337432.9:c.830G>C MANE Select	ENSP00000336701.4:p.Arg277Thr
NM_058216.2:c.830G>C	NP_478123.1:p.Arg277Thr
NR_103872.1:n.734G>C
NR_103872.2:n.705G>C
ENST00000337432.8:c.830G>C	ENSP00000336701.4:p.Arg277Thr
ENST00000413590.5:c.468G>C
ENST00000461271.6:c.479G>C	ENSP00000464056.2:p.Arg160Thr
ENST00000475762.5:c.*1533G>C	ENSP00000432421.1:n.*1533G>C
ENST00000482007.5:c.*258G>C	ENSP00000433332.1:n.*258G>C
ENST00000487525.5:c.*403G>C	ENSP00000431637.1:n.*403G>C
ENST00000578151.1:n.165G>C
ENST00000581221.5:n.345G>C
ENST00000583539.5:c.830G>C	ENSP00000463121.1:p.Arg277Thr
ENST00000584617.5:c.552G>C
ENST00000584804.1:c.125G>C	ENSP00000463658.1:p.Arg42Thr
ENST00000697678.1:n.732G>C
ENST00000697679.1:n.1904G>C
ENST00000697680.1:c.*1694G>C	ENSP00000513392.1:n.*1694G>C
ENST00000697681.1:c.*1991G>C	ENSP00000513393.1:n.*1991G>C
ENST00000697683.1:c.*1694G>C	ENSP00000513395.1:n.*1694G>C
ENST00000697684.1:n.890G>C
ENST00000697685.1:c.*1527G>C	ENSP00000513396.1:n.*1527G>C
ENST00000697686.1:c.479G>C	ENSP00000513397.1:p.Arg160Thr
ENST00000697687.1:n.709G>C
ENST00000697688.1:n.876G>C
ENST00000697689.1:c.*1366G>C	ENSP00000513398.1:n.*1366G>C
ENST00000697690.1:c.830G>C	ENSP00000513399.1:p.Arg277Thr
ENST00000697691.1:c.*802G>C	ENSP00000513400.1:n.*802G>C
ENST00000697692.1:c.*842G>C	ENSP00000513401.1:n.*842G>C
ENST00000697694.1:c.479G>C	ENSP00000513402.1:p.Arg160Thr
ENST00000697695.1:n.1437G>C
XM_006722001.2:c.830G>C	XP_006722064.1:p.Arg277Thr
XM_006722001.4:c.830G>C	XP_006722064.1:p.Arg277Thr
XM_006722002.2:c.830G>C	XP_006722065.1:p.Arg277Thr
XM_006722002.4:c.830G>C	XP_006722065.1:p.Arg277Thr
XM_006722004.2:c.479G>C	XP_006722067.1:p.Arg160Thr
XM_006722004.3:c.479G>C	XP_006722067.1:p.Arg160Thr
XM_006722005.2:c.479G>C	XP_006722068.1:p.Arg160Thr
XM_006722005.3:c.479G>C	XP_006722068.1:p.Arg160Thr
XM_011525092.1:c.479G>C	XP_011523394.1:p.Arg160Thr
XM_011525092.2:c.479G>C	XP_011523394.1:p.Arg160Thr
XM_011525093.1:c.479G>C	XP_011523395.1:p.Arg160Thr
XM_011525093.2:c.479G>C	XP_011523395.1:p.Arg160Thr
XM_011525094.1:c.479G>C	XP_011523396.1:p.Arg160Thr
XM_011525094.2:c.479G>C	XP_011523396.1:p.Arg160Thr
XM_017024914.1:c.479G>C	XP_016880403.1:p.Arg160Thr
XM_017024915.1:c.479G>C	XP_016880404.1:p.Arg160Thr
XM_017024916.1:c.479G>C	XP_016880405.1:p.Arg160Thr
XM_017024917.1:c.479G>C	XP_016880406.1:p.Arg160Thr
XM_017024918.2:c.479G>C	XP_016880407.1:p.Arg160Thr
XM_017024919.1:c.479G>C	XP_016880408.1:p.Arg160Thr
XR_934513.1:n.1048G>C
XR_934513.3:n.1479G>C
XR_934514.1:n.1048G>C
XR_934514.3:n.1479G>C