Canonical Allele Identifier: CA16615463

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58696779T>C , CM000679.2:g.58696779T>C	GRCh38
NC_000017.10:g.56774140T>C , CM000679.1:g.56774140T>C	GRCh37
NC_000017.9:g.54129139T>C	NCBI36
NG_023199.1:g.9178T>C , LRG_314:g.9178T>C
NG_047169.1:g.301A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.491T>C MANE Select	NP_478123.1:p.Phe164Ser
ENST00000337432.9:c.491T>C MANE Select	ENSP00000336701.4:p.Phe164Ser
NM_058216.2:c.491T>C	NP_478123.1:p.Phe164Ser
NR_103872.1:n.475+1590T>C
NR_103872.2:n.446+1590T>C
ENST00000337432.8:c.491T>C	ENSP00000336701.4:p.Phe164Ser
ENST00000413590.5:c.129T>C
ENST00000425173.5:c.287T>C	ENSP00000407282.1:p.Phe96Ser
ENST00000461271.5:c.140T>C	ENSP00000464056.1:p.Phe47Ser
ENST00000461271.6:c.140T>C	ENSP00000464056.2:p.Phe47Ser
ENST00000475762.5:c.*1194T>C	ENSP00000432421.1:n.*1194T>C
ENST00000482007.5:c.404+1590T>C	ENSP00000433332.1:n.404+1590T>C
ENST00000487525.5:c.404+1590T>C	ENSP00000431637.1:n.404+1590T>C
ENST00000487921.5:n.403T>C
ENST00000583539.5:c.491T>C	ENSP00000463121.1:p.Phe164Ser
ENST00000584617.5:c.213T>C
ENST00000622327.4:c.227T>C	ENSP00000482326.1:p.Phe76Ser
ENST00000697675.1:n.3088T>C
ENST00000697676.1:n.551T>C
ENST00000697677.1:n.1572T>C
ENST00000697678.1:n.393T>C
ENST00000697679.1:n.1565T>C
ENST00000697680.1:c.*1355T>C	ENSP00000513392.1:n.*1355T>C
ENST00000697681.1:c.*1382T>C	ENSP00000513393.1:n.*1382T>C
ENST00000697683.1:c.*1355T>C	ENSP00000513395.1:n.*1355T>C
ENST00000697684.1:n.551T>C
ENST00000697685.1:c.*1268+1590T>C	ENSP00000513396.1:n.*1268+1590T>C
ENST00000697686.1:c.140T>C	ENSP00000513397.1:p.Phe47Ser
ENST00000697687.1:n.450+1590T>C
ENST00000697688.1:n.537T>C
ENST00000697689.1:c.*1107+1590T>C	ENSP00000513398.1:n.*1107+1590T>C
ENST00000697690.1:c.491T>C	ENSP00000513399.1:p.Phe164Ser
ENST00000697691.1:c.*463T>C	ENSP00000513400.1:n.*463T>C
ENST00000697692.1:c.*503T>C	ENSP00000513401.1:n.*503T>C
ENST00000697694.1:c.140T>C	ENSP00000513402.1:p.Phe47Ser
ENST00000697695.1:n.1098T>C
XM_006722001.2:c.491T>C	XP_006722064.1:p.Phe164Ser
XM_006722001.4:c.491T>C	XP_006722064.1:p.Phe164Ser
XM_006722002.2:c.491T>C	XP_006722065.1:p.Phe164Ser
XM_006722002.4:c.491T>C	XP_006722065.1:p.Phe164Ser
XM_006722004.2:c.140T>C	XP_006722067.1:p.Phe47Ser
XM_006722004.3:c.140T>C	XP_006722067.1:p.Phe47Ser
XM_006722005.2:c.140T>C	XP_006722068.1:p.Phe47Ser
XM_006722005.3:c.140T>C	XP_006722068.1:p.Phe47Ser
XM_011525092.1:c.140T>C	XP_011523394.1:p.Phe47Ser
XM_011525092.2:c.140T>C	XP_011523394.1:p.Phe47Ser
XM_011525093.1:c.140T>C	XP_011523395.1:p.Phe47Ser
XM_011525093.2:c.140T>C	XP_011523395.1:p.Phe47Ser
XM_011525094.1:c.140T>C	XP_011523396.1:p.Phe47Ser
XM_011525094.2:c.140T>C	XP_011523396.1:p.Phe47Ser
XM_017024914.1:c.140T>C	XP_016880403.1:p.Phe47Ser
XM_017024915.1:c.140T>C	XP_016880404.1:p.Phe47Ser
XM_017024916.1:c.140T>C	XP_016880405.1:p.Phe47Ser
XM_017024917.1:c.140T>C	XP_016880406.1:p.Phe47Ser
XM_017024918.2:c.140T>C	XP_016880407.1:p.Phe47Ser
XM_017024919.1:c.140T>C	XP_016880408.1:p.Phe47Ser
XR_934513.1:n.564T>C
XR_934513.3:n.995T>C
XR_934514.1:n.564T>C
XR_934514.3:n.995T>C