Canonical Allele Identifier: CA626737565

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2673914
• ClinVar RCV Id: RCV003450529
• dbSNP Id: rs1479360028
• gnomAD v2: 17-56801435-AATCTTTC-A
• gnomAD v4: 17-58724074-AATCTTTC-A
• MyVariant Identifiers: chr17:g.56801436_56801442del (hg19) ; chr17:g.58724075_58724081del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724077_58724083del , CM000679.2:g.58724077_58724083del	GRCh38
NC_000017.10:g.56801438_56801444del , CM000679.1:g.56801438_56801444del	GRCh37
NC_000017.9:g.54156437_54156443del	NCBI36
NG_023199.1:g.36476_36482del , LRG_314:g.36476_36482del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.591_597del	ENSP00000464056.2:p.Phe198GlyfsTer?
ENST00000697680.1:c.*1906_*1912del	ENSP00000513392.1:n.*1906_*1912del
ENST00000697681.1:c.*2103_*2109del	ENSP00000513393.1:n.*2103_*2109del
ENST00000697683.1:c.*1806_*1812del	ENSP00000513395.1:n.*1806_*1812del
ENST00000697684.1:n.1002_1008del
ENST00000697685.1:c.*1639_*1645del	ENSP00000513396.1:n.*1639_*1645del
ENST00000697686.1:c.591_597del	ENSP00000513397.1:p.Phe198GlyfsTer?
ENST00000697687.1:n.821_827del
ENST00000697688.1:n.988_994del
ENST00000697689.1:c.*1440+3265_*1440+3271del	ENSP00000513398.1:n.*1440+3265_*1440+3271del
ENST00000697690.1:c.904+3265_904+3271del	ENSP00000513399.1:n.904+3265_904+3271del
ENST00000697691.1:c.*914_*920del	ENSP00000513400.1:n.*914_*920del
ENST00000697692.1:c.*954_*960del	ENSP00000513401.1:n.*954_*960del
ENST00000697694.1:c.591_597del	ENSP00000513402.1:p.Phe198GlyfsTer?
ENST00000697695.1:n.1549_1555del
ENST00000337432.9:c.942_948del MANE Select	ENSP00000336701.4:p.Phe315GlyfsTer?
ENST00000337432.8:c.942_948del	ENSP00000336701.4:p.Phe315GlyfsTer?
ENST00000413590.5:c.580_586del
ENST00000475762.5:c.*1578_*1584del	ENSP00000432421.1:n.*1578_*1584del
ENST00000482007.5:c.*370_*376del	ENSP00000433332.1:n.*370_*376del
ENST00000487525.5:c.*515_*521del	ENSP00000431637.1:n.*515_*521del
ENST00000578151.1:n.239+3265_239+3271del
ENST00000581221.5:n.457_463del
ENST00000583539.5:c.942_948del	ENSP00000463121.1:p.Phe315GlyfsTer?
ENST00000584617.5:c.664_670del
ENST00000584804.1:c.199+3265_199+3271del	ENSP00000463658.1:n.199+3265_199+3271del
NM_058216.2:c.942_948del	NP_478123.1:p.Phe315GlyfsTer?
NR_103872.1:n.846_852del
XM_006722001.2:c.942_948del	XP_006722064.1:p.Phe315GlyfsTer?
XM_006722002.2:c.904+3265_904+3271del	XP_006722065.1:n.904+3265_904+3271del
XM_006722004.2:c.591_597del	XP_006722067.1:p.Phe198GlyfsTer?
XM_006722005.2:c.591_597del	XP_006722068.1:p.Phe198GlyfsTer?
XM_011525092.1:c.591_597del	XP_011523394.1:p.Phe198GlyfsTer?
XM_011525093.1:c.591_597del	XP_011523395.1:p.Phe198GlyfsTer?
XM_011525094.1:c.591_597del	XP_011523396.1:p.Phe198GlyfsTer?
XR_934513.1:n.1160_1166del
XR_934514.1:n.1160_1166del
XM_006722001.4:c.942_948del	XP_006722064.1:p.Phe315GlyfsTer?
XM_006722002.4:c.904+3265_904+3271del	XP_006722065.1:n.904+3265_904+3271del
XM_006722004.3:c.591_597del	XP_006722067.1:p.Phe198GlyfsTer?
XM_006722005.3:c.591_597del	XP_006722068.1:p.Phe198GlyfsTer?
XM_011525092.2:c.591_597del	XP_011523394.1:p.Phe198GlyfsTer?
XM_011525093.2:c.591_597del	XP_011523395.1:p.Phe198GlyfsTer?
XM_011525094.2:c.591_597del	XP_011523396.1:p.Phe198GlyfsTer?
XM_017024914.1:c.591_597del	XP_016880403.1:p.Phe198GlyfsTer?
XM_017024915.1:c.591_597del	XP_016880404.1:p.Phe198GlyfsTer?
XM_017024916.1:c.591_597del	XP_016880405.1:p.Phe198GlyfsTer?
XM_017024917.1:c.591_597del	XP_016880406.1:p.Phe198GlyfsTer?
XM_017024918.2:c.591_597del	XP_016880407.1:p.Phe198GlyfsTer?
XM_017024919.1:c.553+3265_553+3271del	XP_016880408.1:n.553+3265_553+3271del
XR_934513.3:n.1591_1597del
XR_934514.3:n.1591_1597del
NM_058216.3:c.942_948del MANE Select	NP_478123.1:p.Phe315GlyfsTer?
NR_103872.2:n.817_823del