Canonical Allele Identifier: CA400349211

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 3228956
• ClinVar RCV Id: RCV004522583
• gnomAD v4: 17-58703220-T-C
• MyVariant Identifiers: chr17:g.56780581T>C (hg19) ; chr17:g.58703220T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703220T>C , CM000679.2:g.58703220T>C	GRCh38
NC_000017.10:g.56780581T>C , CM000679.1:g.56780581T>C	GRCh37
NC_000017.9:g.54135580T>C	NCBI36
NG_023199.1:g.15619T>C , LRG_314:g.15619T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.245T>C	ENSP00000464056.2:p.Phe82Ser
ENST00000697677.1:n.1677T>C
ENST00000697678.1:n.498T>C
ENST00000697679.1:n.1670T>C
ENST00000697680.1:c.*1460T>C	ENSP00000513392.1:n.*1460T>C
ENST00000697681.1:c.*1612T>C	ENSP00000513393.1:n.*1612T>C
ENST00000697683.1:c.*1460T>C	ENSP00000513395.1:n.*1460T>C
ENST00000697684.1:n.656T>C
ENST00000697685.1:c.*1293T>C	ENSP00000513396.1:n.*1293T>C
ENST00000697686.1:c.245T>C	ENSP00000513397.1:p.Phe82Ser
ENST00000697687.1:n.475T>C
ENST00000697688.1:n.642T>C
ENST00000697689.1:c.*1132T>C	ENSP00000513398.1:n.*1132T>C
ENST00000697690.1:c.596T>C	ENSP00000513399.1:p.Phe199Ser
ENST00000697691.1:c.*568T>C	ENSP00000513400.1:n.*568T>C
ENST00000697692.1:c.*608T>C	ENSP00000513401.1:n.*608T>C
ENST00000697694.1:c.245T>C	ENSP00000513402.1:p.Phe82Ser
ENST00000697695.1:n.1203T>C
ENST00000337432.9:c.596T>C MANE Select	ENSP00000336701.4:p.Phe199Ser
ENST00000337432.8:c.596T>C	ENSP00000336701.4:p.Phe199Ser
ENST00000413590.5:c.234T>C
ENST00000425173.5:c.392T>C	ENSP00000407282.1:p.Phe131Ser
ENST00000461271.5:c.245T>C	ENSP00000464056.1:p.Phe82Ser
ENST00000475762.5:c.*1299T>C	ENSP00000432421.1:n.*1299T>C
ENST00000482007.5:c.*24T>C	ENSP00000433332.1:n.*24T>C
ENST00000487525.5:c.*24T>C	ENSP00000431637.1:n.*24T>C
ENST00000487921.5:n.508T>C
ENST00000583539.5:c.596T>C	ENSP00000463121.1:p.Phe199Ser
ENST00000584617.5:c.318T>C
NM_058216.2:c.596T>C	NP_478123.1:p.Phe199Ser
NR_103872.1:n.500T>C
XM_006722001.2:c.596T>C	XP_006722064.1:p.Phe199Ser
XM_006722002.2:c.596T>C	XP_006722065.1:p.Phe199Ser
XM_006722004.2:c.245T>C	XP_006722067.1:p.Phe82Ser
XM_006722005.2:c.245T>C	XP_006722068.1:p.Phe82Ser
XM_011525092.1:c.245T>C	XP_011523394.1:p.Phe82Ser
XM_011525093.1:c.245T>C	XP_011523395.1:p.Phe82Ser
XM_011525094.1:c.245T>C	XP_011523396.1:p.Phe82Ser
XR_934513.1:n.669T>C
XR_934514.1:n.669T>C
XM_006722001.4:c.596T>C	XP_006722064.1:p.Phe199Ser
XM_006722002.4:c.596T>C	XP_006722065.1:p.Phe199Ser
XM_006722004.3:c.245T>C	XP_006722067.1:p.Phe82Ser
XM_006722005.3:c.245T>C	XP_006722068.1:p.Phe82Ser
XM_011525092.2:c.245T>C	XP_011523394.1:p.Phe82Ser
XM_011525093.2:c.245T>C	XP_011523395.1:p.Phe82Ser
XM_011525094.2:c.245T>C	XP_011523396.1:p.Phe82Ser
XM_017024914.1:c.245T>C	XP_016880403.1:p.Phe82Ser
XM_017024915.1:c.245T>C	XP_016880404.1:p.Phe82Ser
XM_017024916.1:c.245T>C	XP_016880405.1:p.Phe82Ser
XM_017024917.1:c.245T>C	XP_016880406.1:p.Phe82Ser
XM_017024918.2:c.245T>C	XP_016880407.1:p.Phe82Ser
XM_017024919.1:c.245T>C	XP_016880408.1:p.Phe82Ser
XR_934513.3:n.1100T>C
XR_934514.3:n.1100T>C
NM_058216.3:c.596T>C MANE Select	NP_478123.1:p.Phe199Ser
NR_103872.2:n.471T>C