Canonical Allele Identifier: CA400344757

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696771G>T , CM000679.2:g.58696771G>T	GRCh38
NC_000017.10:g.56774132G>T , CM000679.1:g.56774132G>T	GRCh37
NC_000017.9:g.54129131G>T	NCBI36
NG_023199.1:g.9170G>T , LRG_314:g.9170G>T
NG_047169.1:g.309C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.483G>T MANE Select	NP_478123.1:p.Glu161Asp
ENST00000337432.9:c.483G>T MANE Select	ENSP00000336701.4:p.Glu161Asp
NM_058216.2:c.483G>T	NP_478123.1:p.Glu161Asp
NR_103872.1:n.475+1582G>T
NR_103872.2:n.446+1582G>T
ENST00000337432.8:c.483G>T	ENSP00000336701.4:p.Glu161Asp
ENST00000413590.5:c.121G>T
ENST00000425173.5:c.279G>T	ENSP00000407282.1:p.Glu93Asp
ENST00000461271.5:c.132G>T	ENSP00000464056.1:p.Glu44Asp
ENST00000461271.6:c.132G>T	ENSP00000464056.2:p.Glu44Asp
ENST00000475762.5:c.*1186G>T	ENSP00000432421.1:n.*1186G>T
ENST00000482007.5:c.404+1582G>T	ENSP00000433332.1:n.404+1582G>T
ENST00000487525.5:c.404+1582G>T	ENSP00000431637.1:n.404+1582G>T
ENST00000487921.5:n.395G>T
ENST00000583539.5:c.483G>T	ENSP00000463121.1:p.Glu161Asp
ENST00000584617.5:c.205G>T
ENST00000622327.4:c.219G>T	ENSP00000482326.1:p.Glu73Asp
ENST00000697675.1:n.3080G>T
ENST00000697676.1:n.543G>T
ENST00000697677.1:n.1564G>T
ENST00000697678.1:n.385G>T
ENST00000697679.1:n.1557G>T
ENST00000697680.1:c.*1347G>T	ENSP00000513392.1:n.*1347G>T
ENST00000697681.1:c.*1374G>T	ENSP00000513393.1:n.*1374G>T
ENST00000697683.1:c.*1347G>T	ENSP00000513395.1:n.*1347G>T
ENST00000697684.1:n.543G>T
ENST00000697685.1:c.*1268+1582G>T	ENSP00000513396.1:n.*1268+1582G>T
ENST00000697686.1:c.132G>T	ENSP00000513397.1:p.Glu44Asp
ENST00000697687.1:n.450+1582G>T
ENST00000697688.1:n.529G>T
ENST00000697689.1:c.*1107+1582G>T	ENSP00000513398.1:n.*1107+1582G>T
ENST00000697690.1:c.483G>T	ENSP00000513399.1:p.Glu161Asp
ENST00000697691.1:c.*455G>T	ENSP00000513400.1:n.*455G>T
ENST00000697692.1:c.*495G>T	ENSP00000513401.1:n.*495G>T
ENST00000697694.1:c.132G>T	ENSP00000513402.1:p.Glu44Asp
ENST00000697695.1:n.1090G>T
XM_006722001.2:c.483G>T	XP_006722064.1:p.Glu161Asp
XM_006722001.4:c.483G>T	XP_006722064.1:p.Glu161Asp
XM_006722002.2:c.483G>T	XP_006722065.1:p.Glu161Asp
XM_006722002.4:c.483G>T	XP_006722065.1:p.Glu161Asp
XM_006722004.2:c.132G>T	XP_006722067.1:p.Glu44Asp
XM_006722004.3:c.132G>T	XP_006722067.1:p.Glu44Asp
XM_006722005.2:c.132G>T	XP_006722068.1:p.Glu44Asp
XM_006722005.3:c.132G>T	XP_006722068.1:p.Glu44Asp
XM_011525092.1:c.132G>T	XP_011523394.1:p.Glu44Asp
XM_011525092.2:c.132G>T	XP_011523394.1:p.Glu44Asp
XM_011525093.1:c.132G>T	XP_011523395.1:p.Glu44Asp
XM_011525093.2:c.132G>T	XP_011523395.1:p.Glu44Asp
XM_011525094.1:c.132G>T	XP_011523396.1:p.Glu44Asp
XM_011525094.2:c.132G>T	XP_011523396.1:p.Glu44Asp
XM_017024914.1:c.132G>T	XP_016880403.1:p.Glu44Asp
XM_017024915.1:c.132G>T	XP_016880404.1:p.Glu44Asp
XM_017024916.1:c.132G>T	XP_016880405.1:p.Glu44Asp
XM_017024917.1:c.132G>T	XP_016880406.1:p.Glu44Asp
XM_017024918.2:c.132G>T	XP_016880407.1:p.Glu44Asp
XM_017024919.1:c.132G>T	XP_016880408.1:p.Glu44Asp
XR_934513.1:n.556G>T
XR_934513.3:n.987G>T
XR_934514.1:n.556G>T
XR_934514.3:n.987G>T