Canonical Allele Identifier: CA400353999

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709938T>A , CM000679.2:g.58709938T>A	GRCh38
NC_000017.10:g.56787299T>A , CM000679.1:g.56787299T>A	GRCh37
NC_000017.9:g.54142298T>A	NCBI36
NG_023199.1:g.22337T>A , LRG_314:g.22337T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.785T>A MANE Select	NP_478123.1:p.Leu262Ter
ENST00000337432.9:c.785T>A MANE Select	ENSP00000336701.4:p.Leu262Ter
NM_058216.2:c.785T>A	NP_478123.1:p.Leu262Ter
NR_103872.1:n.689T>A
NR_103872.2:n.660T>A
ENST00000337432.8:c.785T>A	ENSP00000336701.4:p.Leu262Ter
ENST00000413590.5:c.423T>A
ENST00000461271.6:c.434T>A	ENSP00000464056.2:p.Leu145Ter
ENST00000475762.5:c.*1488T>A	ENSP00000432421.1:n.*1488T>A
ENST00000482007.5:c.*213T>A	ENSP00000433332.1:n.*213T>A
ENST00000487525.5:c.*358T>A	ENSP00000431637.1:n.*358T>A
ENST00000578151.1:n.120T>A
ENST00000581221.5:n.300T>A
ENST00000583539.5:c.785T>A	ENSP00000463121.1:p.Leu262Ter
ENST00000584617.5:c.507T>A
ENST00000584804.1:c.80T>A	ENSP00000463658.1:p.Leu27Ter
ENST00000697678.1:n.687T>A
ENST00000697679.1:n.1859T>A
ENST00000697680.1:c.*1649T>A	ENSP00000513392.1:n.*1649T>A
ENST00000697681.1:c.*1946T>A	ENSP00000513393.1:n.*1946T>A
ENST00000697683.1:c.*1649T>A	ENSP00000513395.1:n.*1649T>A
ENST00000697684.1:n.845T>A
ENST00000697685.1:c.*1482T>A	ENSP00000513396.1:n.*1482T>A
ENST00000697686.1:c.434T>A	ENSP00000513397.1:p.Leu145Ter
ENST00000697687.1:n.664T>A
ENST00000697688.1:n.831T>A
ENST00000697689.1:c.*1321T>A	ENSP00000513398.1:n.*1321T>A
ENST00000697690.1:c.785T>A	ENSP00000513399.1:p.Leu262Ter
ENST00000697691.1:c.*757T>A	ENSP00000513400.1:n.*757T>A
ENST00000697692.1:c.*797T>A	ENSP00000513401.1:n.*797T>A
ENST00000697694.1:c.434T>A	ENSP00000513402.1:p.Leu145Ter
ENST00000697695.1:n.1392T>A
XM_006722001.2:c.785T>A	XP_006722064.1:p.Leu262Ter
XM_006722001.4:c.785T>A	XP_006722064.1:p.Leu262Ter
XM_006722002.2:c.785T>A	XP_006722065.1:p.Leu262Ter
XM_006722002.4:c.785T>A	XP_006722065.1:p.Leu262Ter
XM_006722004.2:c.434T>A	XP_006722067.1:p.Leu145Ter
XM_006722004.3:c.434T>A	XP_006722067.1:p.Leu145Ter
XM_006722005.2:c.434T>A	XP_006722068.1:p.Leu145Ter
XM_006722005.3:c.434T>A	XP_006722068.1:p.Leu145Ter
XM_011525092.1:c.434T>A	XP_011523394.1:p.Leu145Ter
XM_011525092.2:c.434T>A	XP_011523394.1:p.Leu145Ter
XM_011525093.1:c.434T>A	XP_011523395.1:p.Leu145Ter
XM_011525093.2:c.434T>A	XP_011523395.1:p.Leu145Ter
XM_011525094.1:c.434T>A	XP_011523396.1:p.Leu145Ter
XM_011525094.2:c.434T>A	XP_011523396.1:p.Leu145Ter
XM_017024914.1:c.434T>A	XP_016880403.1:p.Leu145Ter
XM_017024915.1:c.434T>A	XP_016880404.1:p.Leu145Ter
XM_017024916.1:c.434T>A	XP_016880405.1:p.Leu145Ter
XM_017024917.1:c.434T>A	XP_016880406.1:p.Leu145Ter
XM_017024918.2:c.434T>A	XP_016880407.1:p.Leu145Ter
XM_017024919.1:c.434T>A	XP_016880408.1:p.Leu145Ter
XR_934513.1:n.1003T>A
XR_934513.3:n.1434T>A
XR_934514.1:n.1003T>A
XR_934514.3:n.1434T>A