Canonical Allele Identifier: CA400353909

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709929C>G , CM000679.2:g.58709929C>G	GRCh38
NC_000017.10:g.56787290C>G , CM000679.1:g.56787290C>G	GRCh37
NC_000017.9:g.54142289C>G	NCBI36
NG_023199.1:g.22328C>G , LRG_314:g.22328C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.776C>G MANE Select	NP_478123.1:p.Thr259Ser
ENST00000337432.9:c.776C>G MANE Select	ENSP00000336701.4:p.Thr259Ser
NM_058216.2:c.776C>G	NP_478123.1:p.Thr259Ser
NR_103872.1:n.680C>G
NR_103872.2:n.651C>G
ENST00000337432.8:c.776C>G	ENSP00000336701.4:p.Thr259Ser
ENST00000413590.5:c.414C>G
ENST00000461271.6:c.425C>G	ENSP00000464056.2:p.Thr142Ser
ENST00000475762.5:c.*1479C>G	ENSP00000432421.1:n.*1479C>G
ENST00000482007.5:c.*204C>G	ENSP00000433332.1:n.*204C>G
ENST00000487525.5:c.*349C>G	ENSP00000431637.1:n.*349C>G
ENST00000578151.1:n.111C>G
ENST00000581221.5:n.291C>G
ENST00000583539.5:c.776C>G	ENSP00000463121.1:p.Thr259Ser
ENST00000584617.5:c.498C>G
ENST00000584804.1:c.71C>G	ENSP00000463658.1:p.Thr24Ser
ENST00000697678.1:n.678C>G
ENST00000697679.1:n.1850C>G
ENST00000697680.1:c.*1640C>G	ENSP00000513392.1:n.*1640C>G
ENST00000697681.1:c.*1937C>G	ENSP00000513393.1:n.*1937C>G
ENST00000697683.1:c.*1640C>G	ENSP00000513395.1:n.*1640C>G
ENST00000697684.1:n.836C>G
ENST00000697685.1:c.*1473C>G	ENSP00000513396.1:n.*1473C>G
ENST00000697686.1:c.425C>G	ENSP00000513397.1:p.Thr142Ser
ENST00000697687.1:n.655C>G
ENST00000697688.1:n.822C>G
ENST00000697689.1:c.*1312C>G	ENSP00000513398.1:n.*1312C>G
ENST00000697690.1:c.776C>G	ENSP00000513399.1:p.Thr259Ser
ENST00000697691.1:c.*748C>G	ENSP00000513400.1:n.*748C>G
ENST00000697692.1:c.*788C>G	ENSP00000513401.1:n.*788C>G
ENST00000697694.1:c.425C>G	ENSP00000513402.1:p.Thr142Ser
ENST00000697695.1:n.1383C>G
XM_006722001.2:c.776C>G	XP_006722064.1:p.Thr259Ser
XM_006722001.4:c.776C>G	XP_006722064.1:p.Thr259Ser
XM_006722002.2:c.776C>G	XP_006722065.1:p.Thr259Ser
XM_006722002.4:c.776C>G	XP_006722065.1:p.Thr259Ser
XM_006722004.2:c.425C>G	XP_006722067.1:p.Thr142Ser
XM_006722004.3:c.425C>G	XP_006722067.1:p.Thr142Ser
XM_006722005.2:c.425C>G	XP_006722068.1:p.Thr142Ser
XM_006722005.3:c.425C>G	XP_006722068.1:p.Thr142Ser
XM_011525092.1:c.425C>G	XP_011523394.1:p.Thr142Ser
XM_011525092.2:c.425C>G	XP_011523394.1:p.Thr142Ser
XM_011525093.1:c.425C>G	XP_011523395.1:p.Thr142Ser
XM_011525093.2:c.425C>G	XP_011523395.1:p.Thr142Ser
XM_011525094.1:c.425C>G	XP_011523396.1:p.Thr142Ser
XM_011525094.2:c.425C>G	XP_011523396.1:p.Thr142Ser
XM_017024914.1:c.425C>G	XP_016880403.1:p.Thr142Ser
XM_017024915.1:c.425C>G	XP_016880404.1:p.Thr142Ser
XM_017024916.1:c.425C>G	XP_016880405.1:p.Thr142Ser
XM_017024917.1:c.425C>G	XP_016880406.1:p.Thr142Ser
XM_017024918.2:c.425C>G	XP_016880407.1:p.Thr142Ser
XM_017024919.1:c.425C>G	XP_016880408.1:p.Thr142Ser
XR_934513.1:n.994C>G
XR_934513.3:n.1425C>G
XR_934514.1:n.994C>G
XR_934514.3:n.1425C>G