Canonical Allele Identifier: CA400353538

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 958054
• ClinVar RCV Id: RCV001231143
• dbSNP Id: rs531540031
• MyVariant Identifiers: chr17:g.56787262C>G (hg19) ; chr17:g.58709901C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709901C>G , CM000679.2:g.58709901C>G	GRCh38
NC_000017.10:g.56787262C>G , CM000679.1:g.56787262C>G	GRCh37
NC_000017.9:g.54142261C>G	NCBI36
NG_023199.1:g.22300C>G , LRG_314:g.22300C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.397C>G	ENSP00000464056.2:p.His133Asp
ENST00000697678.1:n.650C>G
ENST00000697679.1:n.1822C>G
ENST00000697680.1:c.*1612C>G	ENSP00000513392.1:n.*1612C>G
ENST00000697681.1:c.*1909C>G	ENSP00000513393.1:n.*1909C>G
ENST00000697683.1:c.*1612C>G	ENSP00000513395.1:n.*1612C>G
ENST00000697684.1:n.808C>G
ENST00000697685.1:c.*1445C>G	ENSP00000513396.1:n.*1445C>G
ENST00000697686.1:c.397C>G	ENSP00000513397.1:p.His133Asp
ENST00000697687.1:n.627C>G
ENST00000697688.1:n.794C>G
ENST00000697689.1:c.*1284C>G	ENSP00000513398.1:n.*1284C>G
ENST00000697690.1:c.748C>G	ENSP00000513399.1:p.His250Asp
ENST00000697691.1:c.*720C>G	ENSP00000513400.1:n.*720C>G
ENST00000697692.1:c.*760C>G	ENSP00000513401.1:n.*760C>G
ENST00000697694.1:c.397C>G	ENSP00000513402.1:p.His133Asp
ENST00000697695.1:n.1355C>G
ENST00000337432.9:c.748C>G MANE Select	ENSP00000336701.4:p.His250Asp
ENST00000337432.8:c.748C>G	ENSP00000336701.4:p.His250Asp
ENST00000413590.5:c.386C>G
ENST00000461271.5:c.397C>G	ENSP00000464056.1:p.His133Asp
ENST00000475762.5:c.*1451C>G	ENSP00000432421.1:n.*1451C>G
ENST00000482007.5:c.*176C>G	ENSP00000433332.1:n.*176C>G
ENST00000487525.5:c.*321C>G	ENSP00000431637.1:n.*321C>G
ENST00000578151.1:n.83C>G
ENST00000581221.5:n.263C>G
ENST00000583539.5:c.748C>G	ENSP00000463121.1:p.His250Asp
ENST00000584617.5:c.470C>G
ENST00000584804.1:c.43C>G	ENSP00000463658.1:p.His15Asp
NM_058216.2:c.748C>G	NP_478123.1:p.His250Asp
NR_103872.1:n.652C>G
XM_006722001.2:c.748C>G	XP_006722064.1:p.His250Asp
XM_006722002.2:c.748C>G	XP_006722065.1:p.His250Asp
XM_006722004.2:c.397C>G	XP_006722067.1:p.His133Asp
XM_006722005.2:c.397C>G	XP_006722068.1:p.His133Asp
XM_011525092.1:c.397C>G	XP_011523394.1:p.His133Asp
XM_011525093.1:c.397C>G	XP_011523395.1:p.His133Asp
XM_011525094.1:c.397C>G	XP_011523396.1:p.His133Asp
XR_934513.1:n.966C>G
XR_934514.1:n.966C>G
XM_006722001.4:c.748C>G	XP_006722064.1:p.His250Asp
XM_006722002.4:c.748C>G	XP_006722065.1:p.His250Asp
XM_006722004.3:c.397C>G	XP_006722067.1:p.His133Asp
XM_006722005.3:c.397C>G	XP_006722068.1:p.His133Asp
XM_011525092.2:c.397C>G	XP_011523394.1:p.His133Asp
XM_011525093.2:c.397C>G	XP_011523395.1:p.His133Asp
XM_011525094.2:c.397C>G	XP_011523396.1:p.His133Asp
XM_017024914.1:c.397C>G	XP_016880403.1:p.His133Asp
XM_017024915.1:c.397C>G	XP_016880404.1:p.His133Asp
XM_017024916.1:c.397C>G	XP_016880405.1:p.His133Asp
XM_017024917.1:c.397C>G	XP_016880406.1:p.His133Asp
XM_017024918.2:c.397C>G	XP_016880407.1:p.His133Asp
XM_017024919.1:c.397C>G	XP_016880408.1:p.His133Asp
XR_934513.3:n.1397C>G
XR_934514.3:n.1397C>G
NM_058216.3:c.748C>G MANE Select	NP_478123.1:p.His250Asp
NR_103872.2:n.623C>G