Canonical Allele Identifier: CA8677228

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696739G>A , CM000679.2:g.58696739G>A	GRCh38
NC_000017.10:g.56774100G>A , CM000679.1:g.56774100G>A	GRCh37
NC_000017.9:g.54129099G>A	NCBI36
NG_023199.1:g.9138G>A , LRG_314:g.9138G>A
NG_047169.1:g.341C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.451G>A MANE Select	NP_478123.1:p.Val151Met
ENST00000337432.9:c.451G>A MANE Select	ENSP00000336701.4:p.Val151Met
NM_058216.2:c.451G>A	NP_478123.1:p.Val151Met
NR_103872.1:n.475+1550G>A
NR_103872.2:n.446+1550G>A
ENST00000337432.8:c.451G>A	ENSP00000336701.4:p.Val151Met
ENST00000413590.5:c.89G>A
ENST00000425173.5:c.247G>A	ENSP00000407282.1:p.Val83Met
ENST00000461271.5:c.100G>A	ENSP00000464056.1:p.Val34Met
ENST00000461271.6:c.100G>A	ENSP00000464056.2:p.Val34Met
ENST00000475762.5:c.*1154G>A	ENSP00000432421.1:n.*1154G>A
ENST00000482007.5:c.404+1550G>A	ENSP00000433332.1:n.404+1550G>A
ENST00000487525.5:c.404+1550G>A	ENSP00000431637.1:n.404+1550G>A
ENST00000487921.5:n.363G>A
ENST00000583539.5:c.451G>A	ENSP00000463121.1:p.Val151Met
ENST00000584617.5:c.173G>A
ENST00000622327.4:c.187G>A	ENSP00000482326.1:p.Val63Met
ENST00000697675.1:n.3048G>A
ENST00000697676.1:n.511G>A
ENST00000697677.1:n.1532G>A
ENST00000697678.1:n.353G>A
ENST00000697679.1:n.1525G>A
ENST00000697680.1:c.*1315G>A	ENSP00000513392.1:n.*1315G>A
ENST00000697681.1:c.*1342G>A	ENSP00000513393.1:n.*1342G>A
ENST00000697683.1:c.*1315G>A	ENSP00000513395.1:n.*1315G>A
ENST00000697684.1:n.511G>A
ENST00000697685.1:c.*1268+1550G>A	ENSP00000513396.1:n.*1268+1550G>A
ENST00000697686.1:c.100G>A	ENSP00000513397.1:p.Val34Met
ENST00000697687.1:n.450+1550G>A
ENST00000697688.1:n.497G>A
ENST00000697689.1:c.*1107+1550G>A	ENSP00000513398.1:n.*1107+1550G>A
ENST00000697690.1:c.451G>A	ENSP00000513399.1:p.Val151Met
ENST00000697691.1:c.*423G>A	ENSP00000513400.1:n.*423G>A
ENST00000697692.1:c.*463G>A	ENSP00000513401.1:n.*463G>A
ENST00000697694.1:c.100G>A	ENSP00000513402.1:p.Val34Met
ENST00000697695.1:n.1058G>A
XM_006722001.2:c.451G>A	XP_006722064.1:p.Val151Met
XM_006722001.4:c.451G>A	XP_006722064.1:p.Val151Met
XM_006722002.2:c.451G>A	XP_006722065.1:p.Val151Met
XM_006722002.4:c.451G>A	XP_006722065.1:p.Val151Met
XM_006722004.2:c.100G>A	XP_006722067.1:p.Val34Met
XM_006722004.3:c.100G>A	XP_006722067.1:p.Val34Met
XM_006722005.2:c.100G>A	XP_006722068.1:p.Val34Met
XM_006722005.3:c.100G>A	XP_006722068.1:p.Val34Met
XM_011525092.1:c.100G>A	XP_011523394.1:p.Val34Met
XM_011525092.2:c.100G>A	XP_011523394.1:p.Val34Met
XM_011525093.1:c.100G>A	XP_011523395.1:p.Val34Met
XM_011525093.2:c.100G>A	XP_011523395.1:p.Val34Met
XM_011525094.1:c.100G>A	XP_011523396.1:p.Val34Met
XM_011525094.2:c.100G>A	XP_011523396.1:p.Val34Met
XM_017024914.1:c.100G>A	XP_016880403.1:p.Val34Met
XM_017024915.1:c.100G>A	XP_016880404.1:p.Val34Met
XM_017024916.1:c.100G>A	XP_016880405.1:p.Val34Met
XM_017024917.1:c.100G>A	XP_016880406.1:p.Val34Met
XM_017024918.2:c.100G>A	XP_016880407.1:p.Val34Met
XM_017024919.1:c.100G>A	XP_016880408.1:p.Val34Met
XR_934513.1:n.524G>A
XR_934513.3:n.955G>A
XR_934514.1:n.524G>A
XR_934514.3:n.955G>A