Canonical Allele Identifier: CA400354329

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 484736
• ClinVar RCV Id: RCV000562790 ; RCV001858343
• dbSNP Id: rs1555599262
• gnomAD v4: 17-58709971-C-T
• MyVariant Identifiers: chr17:g.56787332C>T (hg19) ; chr17:g.58709971C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709971C>T , CM000679.2:g.58709971C>T	GRCh38
NC_000017.10:g.56787332C>T , CM000679.1:g.56787332C>T	GRCh37
NC_000017.9:g.54142331C>T	NCBI36
NG_023199.1:g.22370C>T , LRG_314:g.22370C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.467C>T	ENSP00000464056.2:p.Ala156Val
ENST00000697678.1:n.720C>T
ENST00000697679.1:n.1892C>T
ENST00000697680.1:c.*1682C>T	ENSP00000513392.1:n.*1682C>T
ENST00000697681.1:c.*1979C>T	ENSP00000513393.1:n.*1979C>T
ENST00000697683.1:c.*1682C>T	ENSP00000513395.1:n.*1682C>T
ENST00000697684.1:n.878C>T
ENST00000697685.1:c.*1515C>T	ENSP00000513396.1:n.*1515C>T
ENST00000697686.1:c.467C>T	ENSP00000513397.1:p.Ala156Val
ENST00000697687.1:n.697C>T
ENST00000697688.1:n.864C>T
ENST00000697689.1:c.*1354C>T	ENSP00000513398.1:n.*1354C>T
ENST00000697690.1:c.818C>T	ENSP00000513399.1:p.Ala273Val
ENST00000697691.1:c.*790C>T	ENSP00000513400.1:n.*790C>T
ENST00000697692.1:c.*830C>T	ENSP00000513401.1:n.*830C>T
ENST00000697694.1:c.467C>T	ENSP00000513402.1:p.Ala156Val
ENST00000697695.1:n.1425C>T
ENST00000337432.9:c.818C>T MANE Select	ENSP00000336701.4:p.Ala273Val
ENST00000337432.8:c.818C>T	ENSP00000336701.4:p.Ala273Val
ENST00000413590.5:c.456C>T
ENST00000475762.5:c.*1521C>T	ENSP00000432421.1:n.*1521C>T
ENST00000482007.5:c.*246C>T	ENSP00000433332.1:n.*246C>T
ENST00000487525.5:c.*391C>T	ENSP00000431637.1:n.*391C>T
ENST00000578151.1:n.153C>T
ENST00000581221.5:n.333C>T
ENST00000583539.5:c.818C>T	ENSP00000463121.1:p.Ala273Val
ENST00000584617.5:c.540C>T
ENST00000584804.1:c.113C>T	ENSP00000463658.1:p.Ala38Val
NM_058216.2:c.818C>T	NP_478123.1:p.Ala273Val
NR_103872.1:n.722C>T
XM_006722001.2:c.818C>T	XP_006722064.1:p.Ala273Val
XM_006722002.2:c.818C>T	XP_006722065.1:p.Ala273Val
XM_006722004.2:c.467C>T	XP_006722067.1:p.Ala156Val
XM_006722005.2:c.467C>T	XP_006722068.1:p.Ala156Val
XM_011525092.1:c.467C>T	XP_011523394.1:p.Ala156Val
XM_011525093.1:c.467C>T	XP_011523395.1:p.Ala156Val
XM_011525094.1:c.467C>T	XP_011523396.1:p.Ala156Val
XR_934513.1:n.1036C>T
XR_934514.1:n.1036C>T
XM_006722001.4:c.818C>T	XP_006722064.1:p.Ala273Val
XM_006722002.4:c.818C>T	XP_006722065.1:p.Ala273Val
XM_006722004.3:c.467C>T	XP_006722067.1:p.Ala156Val
XM_006722005.3:c.467C>T	XP_006722068.1:p.Ala156Val
XM_011525092.2:c.467C>T	XP_011523394.1:p.Ala156Val
XM_011525093.2:c.467C>T	XP_011523395.1:p.Ala156Val
XM_011525094.2:c.467C>T	XP_011523396.1:p.Ala156Val
XM_017024914.1:c.467C>T	XP_016880403.1:p.Ala156Val
XM_017024915.1:c.467C>T	XP_016880404.1:p.Ala156Val
XM_017024916.1:c.467C>T	XP_016880405.1:p.Ala156Val
XM_017024917.1:c.467C>T	XP_016880406.1:p.Ala156Val
XM_017024918.2:c.467C>T	XP_016880407.1:p.Ala156Val
XM_017024919.1:c.467C>T	XP_016880408.1:p.Ala156Val
XR_934513.3:n.1467C>T
XR_934514.3:n.1467C>T
NM_058216.3:c.818C>T MANE Select	NP_478123.1:p.Ala273Val
NR_103872.2:n.693C>T