Canonical Allele Identifier: CA400340934

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 538765
• ClinVar RCV Id: RCV000648225 ; RCV001191944 ; RCV003459546
• dbSNP Id: rs1060502586
• gnomAD v4: 17-58695078-G-T
• MyVariant Identifiers: chr17:g.56772439G>T (hg19) ; chr17:g.58695078G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695078G>T , CM000679.2:g.58695078G>T	GRCh38
NC_000017.10:g.56772439G>T , CM000679.1:g.56772439G>T	GRCh37
NC_000017.9:g.54127438G>T	NCBI36
NG_023199.1:g.7477G>T , LRG_314:g.7477G>T
NG_047169.1:g.2002C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-59G>T	ENSP00000464056.2:n.-59G>T
ENST00000697675.1:n.1387G>T
ENST00000697676.1:n.353G>T
ENST00000697677.1:n.1374G>T
ENST00000697678.1:n.195G>T
ENST00000697679.1:n.1367G>T
ENST00000697680.1:c.*1157G>T	ENSP00000513392.1:n.*1157G>T
ENST00000697681.1:c.*1157G>T	ENSP00000513393.1:n.*1157G>T
ENST00000697683.1:c.*1157G>T	ENSP00000513395.1:n.*1157G>T
ENST00000697684.1:n.353G>T
ENST00000697685.1:c.*1157G>T	ENSP00000513396.1:n.*1157G>T
ENST00000697686.1:c.-59G>T	ENSP00000513397.1:n.-59G>T
ENST00000697687.1:n.339G>T
ENST00000697688.1:n.339G>T
ENST00000697689.1:c.*996G>T	ENSP00000513398.1:n.*996G>T
ENST00000697690.1:c.293G>T	ENSP00000513399.1:p.Gly98Val
ENST00000697691.1:c.*265G>T	ENSP00000513400.1:n.*265G>T
ENST00000697692.1:c.*305G>T	ENSP00000513401.1:n.*305G>T
ENST00000697693.1:n.1068G>T
ENST00000697694.1:c.-59G>T	ENSP00000513402.1:n.-59G>T
ENST00000697695.1:n.900G>T
ENST00000337432.9:c.293G>T MANE Select	ENSP00000336701.4:p.Gly98Val
ENST00000337432.8:c.293G>T	ENSP00000336701.4:p.Gly98Val
ENST00000421782.3:c.293G>T	ENSP00000391450.2:p.Gly98Val
ENST00000425173.5:c.89G>T	ENSP00000407282.1:p.Gly30Val
ENST00000461271.5:c.-59G>T	ENSP00000464056.1:n.-59G>T
ENST00000475762.5:c.*996G>T	ENSP00000432421.1:n.*996G>T
ENST00000482007.5:c.293G>T	ENSP00000433332.1:p.Gly98Val
ENST00000486827.1:c.*1157G>T	ENSP00000436761.1:n.*1157G>T
ENST00000487525.5:c.293G>T	ENSP00000431637.1:p.Gly98Val
ENST00000487921.5:n.205G>T
ENST00000583539.5:c.293G>T	ENSP00000463121.1:p.Gly98Val
ENST00000584617.5:c.127-1615G>T
ENST00000622327.4:c.29G>T	ENSP00000482326.1:p.Gly10Val
NM_002876.3:c.293G>T	NP_002867.1:p.Gly98Val
NM_058216.2:c.293G>T	NP_478123.1:p.Gly98Val
NR_103872.1:n.364G>T
NR_103873.1:n.261G>T
XM_006722001.2:c.293G>T	XP_006722064.1:p.Gly98Val
XM_006722002.2:c.293G>T	XP_006722065.1:p.Gly98Val
XM_006722004.2:c.-59G>T	XP_006722067.1:n.-59G>T
XM_006722005.2:c.-59G>T	XP_006722068.1:n.-59G>T
XM_011525092.1:c.-59G>T	XP_011523394.1:n.-59G>T
XM_011525093.1:c.-59G>T	XP_011523395.1:n.-59G>T
XM_011525094.1:c.-59G>T	XP_011523396.1:n.-59G>T
XR_934513.1:n.366G>T
XR_934514.1:n.366G>T
XM_006722001.4:c.293G>T	XP_006722064.1:p.Gly98Val
XM_006722002.4:c.293G>T	XP_006722065.1:p.Gly98Val
XM_006722004.3:c.-59G>T	XP_006722067.1:n.-59G>T
XM_006722005.3:c.-59G>T	XP_006722068.1:n.-59G>T
XM_011525092.2:c.-59G>T	XP_011523394.1:n.-59G>T
XM_011525093.2:c.-59G>T	XP_011523395.1:n.-59G>T
XM_011525094.2:c.-59G>T	XP_011523396.1:n.-59G>T
XM_017024914.1:c.-59G>T	XP_016880403.1:n.-59G>T
XM_017024915.1:c.-59G>T	XP_016880404.1:n.-59G>T
XM_017024916.1:c.-59G>T	XP_016880405.1:n.-59G>T
XM_017024917.1:c.-59G>T	XP_016880406.1:n.-59G>T
XM_017024918.2:c.-59G>T	XP_016880407.1:n.-59G>T
XM_017024919.1:c.-59G>T	XP_016880408.1:n.-59G>T
XR_934513.3:n.797G>T
XR_934514.3:n.797G>T
NM_058216.3:c.293G>T MANE Select	NP_478123.1:p.Gly98Val
NR_103872.2:n.335G>T
NM_002876.4:c.293G>T	NP_002867.1:p.Gly98Val