Canonical Allele Identifier: CA400366530

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58734197C>T , CM000679.2:g.58734197C>T	GRCh38
NC_000017.10:g.56811558C>T , CM000679.1:g.56811558C>T	GRCh37
NC_000017.9:g.54166557C>T	NCBI36
NG_023199.1:g.46596C>T , LRG_314:g.46596C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.1106C>T MANE Select	NP_478123.1:p.Ser369Leu
ENST00000337432.9:c.1106C>T MANE Select	ENSP00000336701.4:p.Ser369Leu
NM_058216.2:c.1106C>T	NP_478123.1:p.Ser369Leu
NR_103872.1:n.1010C>T
NR_103872.2:n.981C>T
ENST00000337432.8:c.1106C>T	ENSP00000336701.4:p.Ser369Leu
ENST00000413590.5:c.747C>T
ENST00000461271.6:c.*1638C>T	ENSP00000464056.2:n.*1638C>T
ENST00000461706.1:n.293C>T
ENST00000475762.5:c.*1742C>T	ENSP00000432421.1:n.*1742C>T
ENST00000482007.5:c.*534C>T	ENSP00000433332.1:n.*534C>T
ENST00000487525.5:c.*682C>T	ENSP00000431637.1:n.*682C>T
ENST00000578151.1:n.319C>T
ENST00000581221.5:n.621C>T
ENST00000584804.1:c.340C>T	ENSP00000463658.1:n.340C>T
ENST00000697680.1:c.*2070C>T	ENSP00000513392.1:n.*2070C>T
ENST00000697681.1:c.*2267C>T	ENSP00000513393.1:n.*2267C>T
ENST00000697683.1:c.*2042C>T	ENSP00000513395.1:n.*2042C>T
ENST00000697685.1:c.*1803C>T	ENSP00000513396.1:n.*1803C>T
ENST00000697686.1:c.*16C>T	ENSP00000513397.1:n.*16C>T
ENST00000697689.1:c.*1520C>T	ENSP00000513398.1:n.*1520C>T
ENST00000697690.1:c.*66C>T	ENSP00000513399.1:n.*66C>T
ENST00000697691.1:c.*1078C>T	ENSP00000513400.1:n.*1078C>T
ENST00000697692.1:c.*1118C>T	ENSP00000513401.1:n.*1118C>T
ENST00000697694.1:c.755C>T	ENSP00000513402.1:p.Ser252Leu
ENST00000697695.1:n.1713C>T
XM_006722001.2:c.1109C>T	XP_006722064.1:p.Ser370Leu
XM_006722001.4:c.1109C>T	XP_006722064.1:p.Ser370Leu
XM_006722002.2:c.*16C>T	XP_006722065.1:n.*16C>T
XM_006722002.4:c.*16C>T	XP_006722065.1:n.*16C>T
XM_006722004.2:c.758C>T	XP_006722067.1:p.Ser253Leu
XM_006722004.3:c.758C>T	XP_006722067.1:p.Ser253Leu
XM_006722005.2:c.758C>T	XP_006722068.1:p.Ser253Leu
XM_006722005.3:c.758C>T	XP_006722068.1:p.Ser253Leu
XM_011525092.1:c.758C>T	XP_011523394.1:p.Ser253Leu
XM_011525092.2:c.758C>T	XP_011523394.1:p.Ser253Leu
XM_011525093.1:c.758C>T	XP_011523395.1:p.Ser253Leu
XM_011525093.2:c.758C>T	XP_011523395.1:p.Ser253Leu
XM_011525094.1:c.758C>T	XP_011523396.1:p.Ser253Leu
XM_011525094.2:c.758C>T	XP_011523396.1:p.Ser253Leu
XM_017024914.1:c.755C>T	XP_016880403.1:p.Ser252Leu
XM_017024915.1:c.755C>T	XP_016880404.1:p.Ser252Leu
XM_017024916.1:c.755C>T	XP_016880405.1:p.Ser252Leu
XM_017024917.1:c.755C>T	XP_016880406.1:p.Ser252Leu
XM_017024918.2:c.755C>T	XP_016880407.1:p.Ser252Leu
XM_017024919.1:c.*16C>T	XP_016880408.1:n.*16C>T
XR_934513.1:n.1324C>T
XR_934513.3:n.1755C>T
XR_934886.1:n.149+3874G>A
XR_934886.2:n.149+3874G>A