Canonical Allele Identifier: CA501075195

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 480495
• ClinVar RCV Id: RCV000565334 ; RCV001421285
• dbSNP Id: rs1555597088
• gnomAD v4: 17-58703212-G-A
• MyVariant Identifiers: chr17:g.56780573G>A (hg19) ; chr17:g.58703212G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703212G>A , CM000679.2:g.58703212G>A	GRCh38
NC_000017.10:g.56780573G>A , CM000679.1:g.56780573G>A	GRCh37
NC_000017.9:g.54135572G>A	NCBI36
NG_023199.1:g.15611G>A , LRG_314:g.15611G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.237G>A	ENSP00000464056.2:p.Leu79=
ENST00000697677.1:n.1669G>A
ENST00000697678.1:n.490G>A
ENST00000697679.1:n.1662G>A
ENST00000697680.1:c.*1452G>A	ENSP00000513392.1:n.*1452G>A
ENST00000697681.1:c.*1604G>A	ENSP00000513393.1:n.*1604G>A
ENST00000697683.1:c.*1452G>A	ENSP00000513395.1:n.*1452G>A
ENST00000697684.1:n.648G>A
ENST00000697685.1:c.*1285G>A	ENSP00000513396.1:n.*1285G>A
ENST00000697686.1:c.237G>A	ENSP00000513397.1:p.Leu79=
ENST00000697687.1:n.467G>A
ENST00000697688.1:n.634G>A
ENST00000697689.1:c.*1124G>A	ENSP00000513398.1:n.*1124G>A
ENST00000697690.1:c.588G>A	ENSP00000513399.1:p.Leu196=
ENST00000697691.1:c.*560G>A	ENSP00000513400.1:n.*560G>A
ENST00000697692.1:c.*600G>A	ENSP00000513401.1:n.*600G>A
ENST00000697694.1:c.237G>A	ENSP00000513402.1:p.Leu79=
ENST00000697695.1:n.1195G>A
ENST00000337432.9:c.588G>A MANE Select	ENSP00000336701.4:p.Leu196=
ENST00000337432.8:c.588G>A	ENSP00000336701.4:p.Leu196=
ENST00000413590.5:c.226G>A
ENST00000425173.5:c.384G>A	ENSP00000407282.1:p.Leu128=
ENST00000461271.5:c.237G>A	ENSP00000464056.1:p.Leu79=
ENST00000475762.5:c.*1291G>A	ENSP00000432421.1:n.*1291G>A
ENST00000482007.5:c.*16G>A	ENSP00000433332.1:n.*16G>A
ENST00000487525.5:c.*16G>A	ENSP00000431637.1:n.*16G>A
ENST00000487921.5:n.500G>A
ENST00000583539.5:c.588G>A	ENSP00000463121.1:p.Leu196=
ENST00000584617.5:c.310G>A
NM_058216.2:c.588G>A	NP_478123.1:p.Leu196=
NR_103872.1:n.492G>A
XM_006722001.2:c.588G>A	XP_006722064.1:p.Leu196=
XM_006722002.2:c.588G>A	XP_006722065.1:p.Leu196=
XM_006722004.2:c.237G>A	XP_006722067.1:p.Leu79=
XM_006722005.2:c.237G>A	XP_006722068.1:p.Leu79=
XM_011525092.1:c.237G>A	XP_011523394.1:p.Leu79=
XM_011525093.1:c.237G>A	XP_011523395.1:p.Leu79=
XM_011525094.1:c.237G>A	XP_011523396.1:p.Leu79=
XR_934513.1:n.661G>A
XR_934514.1:n.661G>A
XM_006722001.4:c.588G>A	XP_006722064.1:p.Leu196=
XM_006722002.4:c.588G>A	XP_006722065.1:p.Leu196=
XM_006722004.3:c.237G>A	XP_006722067.1:p.Leu79=
XM_006722005.3:c.237G>A	XP_006722068.1:p.Leu79=
XM_011525092.2:c.237G>A	XP_011523394.1:p.Leu79=
XM_011525093.2:c.237G>A	XP_011523395.1:p.Leu79=
XM_011525094.2:c.237G>A	XP_011523396.1:p.Leu79=
XM_017024914.1:c.237G>A	XP_016880403.1:p.Leu79=
XM_017024915.1:c.237G>A	XP_016880404.1:p.Leu79=
XM_017024916.1:c.237G>A	XP_016880405.1:p.Leu79=
XM_017024917.1:c.237G>A	XP_016880406.1:p.Leu79=
XM_017024918.2:c.237G>A	XP_016880407.1:p.Leu79=
XM_017024919.1:c.237G>A	XP_016880408.1:p.Leu79=
XR_934513.3:n.1092G>A
XR_934514.3:n.1092G>A
NM_058216.3:c.588G>A MANE Select	NP_478123.1:p.Leu196=
NR_103872.2:n.463G>A