Canonical Allele Identifier: CA8677284

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1692065
• ClinVar RCV Id: RCV002255829 ; RCV003094198
• dbSNP Id: rs775006411
• ExAC: 17:56780609 T / G
• gnomAD v2: 17-56780609-T-G
• MyVariant Identifiers: chr17:g.56780609T>G (hg19) ; chr17:g.58703248T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703248T>G , CM000679.2:g.58703248T>G	GRCh38
NC_000017.10:g.56780609T>G , CM000679.1:g.56780609T>G	GRCh37
NC_000017.9:g.54135608T>G	NCBI36
NG_023199.1:g.15647T>G , LRG_314:g.15647T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.273T>G	ENSP00000464056.2:p.Ile91Met
ENST00000697677.1:n.1705T>G
ENST00000697678.1:n.526T>G
ENST00000697679.1:n.1698T>G
ENST00000697680.1:c.*1488T>G	ENSP00000513392.1:n.*1488T>G
ENST00000697681.1:c.*1640T>G	ENSP00000513393.1:n.*1640T>G
ENST00000697683.1:c.*1488T>G	ENSP00000513395.1:n.*1488T>G
ENST00000697684.1:n.684T>G
ENST00000697685.1:c.*1321T>G	ENSP00000513396.1:n.*1321T>G
ENST00000697686.1:c.273T>G	ENSP00000513397.1:p.Ile91Met
ENST00000697687.1:n.503T>G
ENST00000697688.1:n.670T>G
ENST00000697689.1:c.*1160T>G	ENSP00000513398.1:n.*1160T>G
ENST00000697690.1:c.624T>G	ENSP00000513399.1:p.Ile208Met
ENST00000697691.1:c.*596T>G	ENSP00000513400.1:n.*596T>G
ENST00000697692.1:c.*636T>G	ENSP00000513401.1:n.*636T>G
ENST00000697694.1:c.273T>G	ENSP00000513402.1:p.Ile91Met
ENST00000697695.1:n.1231T>G
ENST00000337432.9:c.624T>G MANE Select	ENSP00000336701.4:p.Ile208Met
ENST00000337432.8:c.624T>G	ENSP00000336701.4:p.Ile208Met
ENST00000413590.5:c.262T>G
ENST00000425173.5:c.420T>G	ENSP00000407282.1:p.Ile140Met
ENST00000461271.5:c.273T>G	ENSP00000464056.1:p.Ile91Met
ENST00000475762.5:c.*1327T>G	ENSP00000432421.1:n.*1327T>G
ENST00000482007.5:c.*52T>G	ENSP00000433332.1:n.*52T>G
ENST00000487525.5:c.*52T>G	ENSP00000431637.1:n.*52T>G
ENST00000487921.5:n.536T>G
ENST00000583539.5:c.624T>G	ENSP00000463121.1:p.Ile208Met
ENST00000584617.5:c.346T>G
NM_058216.2:c.624T>G	NP_478123.1:p.Ile208Met
NR_103872.1:n.528T>G
XM_006722001.2:c.624T>G	XP_006722064.1:p.Ile208Met
XM_006722002.2:c.624T>G	XP_006722065.1:p.Ile208Met
XM_006722004.2:c.273T>G	XP_006722067.1:p.Ile91Met
XM_006722005.2:c.273T>G	XP_006722068.1:p.Ile91Met
XM_011525092.1:c.273T>G	XP_011523394.1:p.Ile91Met
XM_011525093.1:c.273T>G	XP_011523395.1:p.Ile91Met
XM_011525094.1:c.273T>G	XP_011523396.1:p.Ile91Met
XR_934513.1:n.697T>G
XR_934514.1:n.697T>G
XM_006722001.4:c.624T>G	XP_006722064.1:p.Ile208Met
XM_006722002.4:c.624T>G	XP_006722065.1:p.Ile208Met
XM_006722004.3:c.273T>G	XP_006722067.1:p.Ile91Met
XM_006722005.3:c.273T>G	XP_006722068.1:p.Ile91Met
XM_011525092.2:c.273T>G	XP_011523394.1:p.Ile91Met
XM_011525093.2:c.273T>G	XP_011523395.1:p.Ile91Met
XM_011525094.2:c.273T>G	XP_011523396.1:p.Ile91Met
XM_017024914.1:c.273T>G	XP_016880403.1:p.Ile91Met
XM_017024915.1:c.273T>G	XP_016880404.1:p.Ile91Met
XM_017024916.1:c.273T>G	XP_016880405.1:p.Ile91Met
XM_017024917.1:c.273T>G	XP_016880406.1:p.Ile91Met
XM_017024918.2:c.273T>G	XP_016880407.1:p.Ile91Met
XM_017024919.1:c.273T>G	XP_016880408.1:p.Ile91Met
XR_934513.3:n.1128T>G
XR_934514.3:n.1128T>G
NM_058216.3:c.624T>G MANE Select	NP_478123.1:p.Ile208Met
NR_103872.2:n.499T>G