Canonical Allele Identifier: CA400348989

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56780558A>C (hg19) ; chr17:g.58703197A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703197A>C , CM000679.2:g.58703197A>C	GRCh38
NC_000017.10:g.56780558A>C , CM000679.1:g.56780558A>C	GRCh37
NC_000017.9:g.54135557A>C	NCBI36
NG_023199.1:g.15596A>C , LRG_314:g.15596A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.222A>C	ENSP00000464056.2:p.Glu74Asp
ENST00000697677.1:n.1654A>C
ENST00000697678.1:n.475A>C
ENST00000697679.1:n.1647A>C
ENST00000697680.1:c.*1437A>C	ENSP00000513392.1:n.*1437A>C
ENST00000697681.1:c.*1589A>C	ENSP00000513393.1:n.*1589A>C
ENST00000697683.1:c.*1437A>C	ENSP00000513395.1:n.*1437A>C
ENST00000697684.1:n.633A>C
ENST00000697685.1:c.*1270A>C	ENSP00000513396.1:n.*1270A>C
ENST00000697686.1:c.222A>C	ENSP00000513397.1:p.Glu74Asp
ENST00000697687.1:n.452A>C
ENST00000697688.1:n.619A>C
ENST00000697689.1:c.*1109A>C	ENSP00000513398.1:n.*1109A>C
ENST00000697690.1:c.573A>C	ENSP00000513399.1:p.Glu191Asp
ENST00000697691.1:c.*545A>C	ENSP00000513400.1:n.*545A>C
ENST00000697692.1:c.*585A>C	ENSP00000513401.1:n.*585A>C
ENST00000697694.1:c.222A>C	ENSP00000513402.1:p.Glu74Asp
ENST00000697695.1:n.1180A>C
ENST00000337432.9:c.573A>C MANE Select	ENSP00000336701.4:p.Glu191Asp
ENST00000337432.8:c.573A>C	ENSP00000336701.4:p.Glu191Asp
ENST00000413590.5:c.211A>C
ENST00000425173.5:c.369A>C	ENSP00000407282.1:p.Glu123Asp
ENST00000461271.5:c.222A>C	ENSP00000464056.1:p.Glu74Asp
ENST00000475762.5:c.*1276A>C	ENSP00000432421.1:n.*1276A>C
ENST00000482007.5:c.*1A>C	ENSP00000433332.1:n.*1A>C
ENST00000487525.5:c.*1A>C	ENSP00000431637.1:n.*1A>C
ENST00000487921.5:n.485A>C
ENST00000583539.5:c.573A>C	ENSP00000463121.1:p.Glu191Asp
ENST00000584617.5:c.295A>C
NM_058216.2:c.573A>C	NP_478123.1:p.Glu191Asp
NR_103872.1:n.477A>C
XM_006722001.2:c.573A>C	XP_006722064.1:p.Glu191Asp
XM_006722002.2:c.573A>C	XP_006722065.1:p.Glu191Asp
XM_006722004.2:c.222A>C	XP_006722067.1:p.Glu74Asp
XM_006722005.2:c.222A>C	XP_006722068.1:p.Glu74Asp
XM_011525092.1:c.222A>C	XP_011523394.1:p.Glu74Asp
XM_011525093.1:c.222A>C	XP_011523395.1:p.Glu74Asp
XM_011525094.1:c.222A>C	XP_011523396.1:p.Glu74Asp
XR_934513.1:n.646A>C
XR_934514.1:n.646A>C
XM_006722001.4:c.573A>C	XP_006722064.1:p.Glu191Asp
XM_006722002.4:c.573A>C	XP_006722065.1:p.Glu191Asp
XM_006722004.3:c.222A>C	XP_006722067.1:p.Glu74Asp
XM_006722005.3:c.222A>C	XP_006722068.1:p.Glu74Asp
XM_011525092.2:c.222A>C	XP_011523394.1:p.Glu74Asp
XM_011525093.2:c.222A>C	XP_011523395.1:p.Glu74Asp
XM_011525094.2:c.222A>C	XP_011523396.1:p.Glu74Asp
XM_017024914.1:c.222A>C	XP_016880403.1:p.Glu74Asp
XM_017024915.1:c.222A>C	XP_016880404.1:p.Glu74Asp
XM_017024916.1:c.222A>C	XP_016880405.1:p.Glu74Asp
XM_017024917.1:c.222A>C	XP_016880406.1:p.Glu74Asp
XM_017024918.2:c.222A>C	XP_016880407.1:p.Glu74Asp
XM_017024919.1:c.222A>C	XP_016880408.1:p.Glu74Asp
XR_934513.3:n.1077A>C
XR_934514.3:n.1077A>C
NM_058216.3:c.573A>C MANE Select	NP_478123.1:p.Glu191Asp
NR_103872.2:n.448A>C