Canonical Allele Identifier: CA626734869

Gene: RAD51C

Linked Data

• dbSNP Id: rs1567794476
• gnomAD v2: 17-56780686-CAA-C
• gnomAD v4: 17-58703325-CAA-C
• MyVariant Identifiers: chr17:g.56780687_56780688del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703327_58703328del , CM000679.2:g.58703327_58703328del	GRCh38
NC_000017.10:g.56780688_56780689del , CM000679.1:g.56780688_56780689del	GRCh37
NC_000017.9:g.54135687_54135688del	NCBI36
NG_023199.1:g.15726_15727del , LRG_314:g.15726_15727del

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.352_353del	ENSP00000464056.2:p.Lys118GlyfsTer16
ENST00000697677.1:n.1784_1785del
ENST00000697678.1:n.605_606del
ENST00000697679.1:n.1777_1778del
ENST00000697680.1:c.*1567_*1568del	ENSP00000513392.1:n.*1567_*1568del
ENST00000697681.1:c.*1719_*1720del	ENSP00000513393.1:n.*1719_*1720del
ENST00000697683.1:c.*1567_*1568del	ENSP00000513395.1:n.*1567_*1568del
ENST00000697684.1:n.763_764del
ENST00000697685.1:c.*1400_*1401del	ENSP00000513396.1:n.*1400_*1401del
ENST00000697686.1:c.352_353del	ENSP00000513397.1:p.Lys118GlyfsTer16
ENST00000697687.1:n.582_583del
ENST00000697688.1:n.749_750del
ENST00000697689.1:c.*1239_*1240del	ENSP00000513398.1:n.*1239_*1240del
ENST00000697690.1:c.703_704del	ENSP00000513399.1:p.Lys235GlyfsTer16
ENST00000697691.1:c.*675_*676del	ENSP00000513400.1:n.*675_*676del
ENST00000697692.1:c.*715_*716del	ENSP00000513401.1:n.*715_*716del
ENST00000697694.1:c.352_353del	ENSP00000513402.1:p.Lys118GlyfsTer16
ENST00000697695.1:n.1310_1311del
ENST00000337432.9:c.703_704del MANE Select	ENSP00000336701.4:p.Lys235GlyfsTer16
ENST00000337432.8:c.703_704del	ENSP00000336701.4:p.Lys235GlyfsTer16
ENST00000413590.5:c.341_342del
ENST00000425173.5:c.499_500del	ENSP00000407282.1:p.Lys167GlyfsTer5
ENST00000461271.5:c.352_353del	ENSP00000464056.1:p.Lys118GlyfsTer16
ENST00000475762.5:c.*1406_*1407del	ENSP00000432421.1:n.*1406_*1407del
ENST00000482007.5:c.*131_*132del	ENSP00000433332.1:n.*131_*132del
ENST00000487525.5:c.*131_*132del	ENSP00000431637.1:n.*131_*132del
ENST00000487921.5:n.615_616del
ENST00000583539.5:c.703_704del	ENSP00000463121.1:p.Lys235GlyfsTer16
ENST00000584617.5:c.425_426del
NM_058216.2:c.703_704del	NP_478123.1:p.Lys235GlyfsTer16
NR_103872.1:n.607_608del
XM_006722001.2:c.703_704del	XP_006722064.1:p.Lys235GlyfsTer16
XM_006722002.2:c.703_704del	XP_006722065.1:p.Lys235GlyfsTer16
XM_006722004.2:c.352_353del	XP_006722067.1:p.Lys118GlyfsTer16
XM_006722005.2:c.352_353del	XP_006722068.1:p.Lys118GlyfsTer16
XM_011525092.1:c.352_353del	XP_011523394.1:p.Lys118GlyfsTer16
XM_011525093.1:c.352_353del	XP_011523395.1:p.Lys118GlyfsTer16
XM_011525094.1:c.352_353del	XP_011523396.1:p.Lys118GlyfsTer16
XR_934513.1:n.776_777del
XR_934514.1:n.776_777del
XM_006722001.4:c.703_704del	XP_006722064.1:p.Lys235GlyfsTer16
XM_006722002.4:c.703_704del	XP_006722065.1:p.Lys235GlyfsTer16
XM_006722004.3:c.352_353del	XP_006722067.1:p.Lys118GlyfsTer16
XM_006722005.3:c.352_353del	XP_006722068.1:p.Lys118GlyfsTer16
XM_011525092.2:c.352_353del	XP_011523394.1:p.Lys118GlyfsTer16
XM_011525093.2:c.352_353del	XP_011523395.1:p.Lys118GlyfsTer16
XM_011525094.2:c.352_353del	XP_011523396.1:p.Lys118GlyfsTer16
XM_017024914.1:c.352_353del	XP_016880403.1:p.Lys118GlyfsTer16
XM_017024915.1:c.352_353del	XP_016880404.1:p.Lys118GlyfsTer16
XM_017024916.1:c.352_353del	XP_016880405.1:p.Lys118GlyfsTer16
XM_017024917.1:c.352_353del	XP_016880406.1:p.Lys118GlyfsTer16
XM_017024918.2:c.352_353del	XP_016880407.1:p.Lys118GlyfsTer16
XM_017024919.1:c.352_353del	XP_016880408.1:p.Lys118GlyfsTer16
XR_934513.3:n.1207_1208del
XR_934514.3:n.1207_1208del
NM_058216.3:c.703_704del MANE Select	NP_478123.1:p.Lys235GlyfsTer16
NR_103872.2:n.578_579del