Canonical Allele Identifier: CA400354499

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709986T>C , CM000679.2:g.58709986T>C	GRCh38
NC_000017.10:g.56787347T>C , CM000679.1:g.56787347T>C	GRCh37
NC_000017.9:g.54142346T>C	NCBI36
NG_023199.1:g.22385T>C , LRG_314:g.22385T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.833T>C MANE Select	NP_478123.1:p.Leu278Ser
ENST00000337432.9:c.833T>C MANE Select	ENSP00000336701.4:p.Leu278Ser
NM_058216.2:c.833T>C	NP_478123.1:p.Leu278Ser
NR_103872.1:n.737T>C
NR_103872.2:n.708T>C
ENST00000337432.8:c.833T>C	ENSP00000336701.4:p.Leu278Ser
ENST00000413590.5:c.471T>C
ENST00000461271.6:c.482T>C	ENSP00000464056.2:p.Leu161Ser
ENST00000475762.5:c.*1536T>C	ENSP00000432421.1:n.*1536T>C
ENST00000482007.5:c.*261T>C	ENSP00000433332.1:n.*261T>C
ENST00000487525.5:c.*406T>C	ENSP00000431637.1:n.*406T>C
ENST00000578151.1:n.168T>C
ENST00000581221.5:n.348T>C
ENST00000583539.5:c.833T>C	ENSP00000463121.1:p.Leu278Ser
ENST00000584617.5:c.555T>C
ENST00000584804.1:c.128T>C	ENSP00000463658.1:p.Leu43Ser
ENST00000697678.1:n.735T>C
ENST00000697679.1:n.1907T>C
ENST00000697680.1:c.*1697T>C	ENSP00000513392.1:n.*1697T>C
ENST00000697681.1:c.*1994T>C	ENSP00000513393.1:n.*1994T>C
ENST00000697683.1:c.*1697T>C	ENSP00000513395.1:n.*1697T>C
ENST00000697684.1:n.893T>C
ENST00000697685.1:c.*1530T>C	ENSP00000513396.1:n.*1530T>C
ENST00000697686.1:c.482T>C	ENSP00000513397.1:p.Leu161Ser
ENST00000697687.1:n.712T>C
ENST00000697688.1:n.879T>C
ENST00000697689.1:c.*1369T>C	ENSP00000513398.1:n.*1369T>C
ENST00000697690.1:c.833T>C	ENSP00000513399.1:p.Leu278Ser
ENST00000697691.1:c.*805T>C	ENSP00000513400.1:n.*805T>C
ENST00000697692.1:c.*845T>C	ENSP00000513401.1:n.*845T>C
ENST00000697694.1:c.482T>C	ENSP00000513402.1:p.Leu161Ser
ENST00000697695.1:n.1440T>C
XM_006722001.2:c.833T>C	XP_006722064.1:p.Leu278Ser
XM_006722001.4:c.833T>C	XP_006722064.1:p.Leu278Ser
XM_006722002.2:c.833T>C	XP_006722065.1:p.Leu278Ser
XM_006722002.4:c.833T>C	XP_006722065.1:p.Leu278Ser
XM_006722004.2:c.482T>C	XP_006722067.1:p.Leu161Ser
XM_006722004.3:c.482T>C	XP_006722067.1:p.Leu161Ser
XM_006722005.2:c.482T>C	XP_006722068.1:p.Leu161Ser
XM_006722005.3:c.482T>C	XP_006722068.1:p.Leu161Ser
XM_011525092.1:c.482T>C	XP_011523394.1:p.Leu161Ser
XM_011525092.2:c.482T>C	XP_011523394.1:p.Leu161Ser
XM_011525093.1:c.482T>C	XP_011523395.1:p.Leu161Ser
XM_011525093.2:c.482T>C	XP_011523395.1:p.Leu161Ser
XM_011525094.1:c.482T>C	XP_011523396.1:p.Leu161Ser
XM_011525094.2:c.482T>C	XP_011523396.1:p.Leu161Ser
XM_017024914.1:c.482T>C	XP_016880403.1:p.Leu161Ser
XM_017024915.1:c.482T>C	XP_016880404.1:p.Leu161Ser
XM_017024916.1:c.482T>C	XP_016880405.1:p.Leu161Ser
XM_017024917.1:c.482T>C	XP_016880406.1:p.Leu161Ser
XM_017024918.2:c.482T>C	XP_016880407.1:p.Leu161Ser
XM_017024919.1:c.482T>C	XP_016880408.1:p.Leu161Ser
XR_934513.1:n.1051T>C
XR_934513.3:n.1482T>C
XR_934514.1:n.1051T>C
XR_934514.3:n.1482T>C