Canonical Allele Identifier: CA400349417

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1009535
• ClinVar RCV Id: RCV001307041
• dbSNP Id: rs1598473279
• MyVariant Identifiers: chr17:g.56780608T>G (hg19) ; chr17:g.58703247T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703247T>G , CM000679.2:g.58703247T>G	GRCh38
NC_000017.10:g.56780608T>G , CM000679.1:g.56780608T>G	GRCh37
NC_000017.9:g.54135607T>G	NCBI36
NG_023199.1:g.15646T>G , LRG_314:g.15646T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.272T>G	ENSP00000464056.2:p.Ile91Ser
ENST00000697677.1:n.1704T>G
ENST00000697678.1:n.525T>G
ENST00000697679.1:n.1697T>G
ENST00000697680.1:c.*1487T>G	ENSP00000513392.1:n.*1487T>G
ENST00000697681.1:c.*1639T>G	ENSP00000513393.1:n.*1639T>G
ENST00000697683.1:c.*1487T>G	ENSP00000513395.1:n.*1487T>G
ENST00000697684.1:n.683T>G
ENST00000697685.1:c.*1320T>G	ENSP00000513396.1:n.*1320T>G
ENST00000697686.1:c.272T>G	ENSP00000513397.1:p.Ile91Ser
ENST00000697687.1:n.502T>G
ENST00000697688.1:n.669T>G
ENST00000697689.1:c.*1159T>G	ENSP00000513398.1:n.*1159T>G
ENST00000697690.1:c.623T>G	ENSP00000513399.1:p.Ile208Ser
ENST00000697691.1:c.*595T>G	ENSP00000513400.1:n.*595T>G
ENST00000697692.1:c.*635T>G	ENSP00000513401.1:n.*635T>G
ENST00000697694.1:c.272T>G	ENSP00000513402.1:p.Ile91Ser
ENST00000697695.1:n.1230T>G
ENST00000337432.9:c.623T>G MANE Select	ENSP00000336701.4:p.Ile208Ser
ENST00000337432.8:c.623T>G	ENSP00000336701.4:p.Ile208Ser
ENST00000413590.5:c.261T>G
ENST00000425173.5:c.419T>G	ENSP00000407282.1:p.Ile140Ser
ENST00000461271.5:c.272T>G	ENSP00000464056.1:p.Ile91Ser
ENST00000475762.5:c.*1326T>G	ENSP00000432421.1:n.*1326T>G
ENST00000482007.5:c.*51T>G	ENSP00000433332.1:n.*51T>G
ENST00000487525.5:c.*51T>G	ENSP00000431637.1:n.*51T>G
ENST00000487921.5:n.535T>G
ENST00000583539.5:c.623T>G	ENSP00000463121.1:p.Ile208Ser
ENST00000584617.5:c.345T>G
NM_058216.2:c.623T>G	NP_478123.1:p.Ile208Ser
NR_103872.1:n.527T>G
XM_006722001.2:c.623T>G	XP_006722064.1:p.Ile208Ser
XM_006722002.2:c.623T>G	XP_006722065.1:p.Ile208Ser
XM_006722004.2:c.272T>G	XP_006722067.1:p.Ile91Ser
XM_006722005.2:c.272T>G	XP_006722068.1:p.Ile91Ser
XM_011525092.1:c.272T>G	XP_011523394.1:p.Ile91Ser
XM_011525093.1:c.272T>G	XP_011523395.1:p.Ile91Ser
XM_011525094.1:c.272T>G	XP_011523396.1:p.Ile91Ser
XR_934513.1:n.696T>G
XR_934514.1:n.696T>G
XM_006722001.4:c.623T>G	XP_006722064.1:p.Ile208Ser
XM_006722002.4:c.623T>G	XP_006722065.1:p.Ile208Ser
XM_006722004.3:c.272T>G	XP_006722067.1:p.Ile91Ser
XM_006722005.3:c.272T>G	XP_006722068.1:p.Ile91Ser
XM_011525092.2:c.272T>G	XP_011523394.1:p.Ile91Ser
XM_011525093.2:c.272T>G	XP_011523395.1:p.Ile91Ser
XM_011525094.2:c.272T>G	XP_011523396.1:p.Ile91Ser
XM_017024914.1:c.272T>G	XP_016880403.1:p.Ile91Ser
XM_017024915.1:c.272T>G	XP_016880404.1:p.Ile91Ser
XM_017024916.1:c.272T>G	XP_016880405.1:p.Ile91Ser
XM_017024917.1:c.272T>G	XP_016880406.1:p.Ile91Ser
XM_017024918.2:c.272T>G	XP_016880407.1:p.Ile91Ser
XM_017024919.1:c.272T>G	XP_016880408.1:p.Ile91Ser
XR_934513.3:n.1127T>G
XR_934514.3:n.1127T>G
NM_058216.3:c.623T>G MANE Select	NP_478123.1:p.Ile208Ser
NR_103872.2:n.498T>G