Canonical Allele Identifier: CA3261178972
Community Standard Title: NM_058216.3(RAD51C):c.875_876delinsAG (p.Arg292Lys)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58720783_58720784delinsAG , CM000679.2:g.58720783_58720784delinsAG GRCh38
NC_000017.10:g.56798144_56798145delinsAG , CM000679.1:g.56798144_56798145delinsAG GRCh37
NC_000017.9:g.54153143_54153144delinsAG NCBI36
NG_023199.1:g.33182_33183delinsAG , LRG_314:g.33182_33183delinsAG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.875_876delinsAG MANE Select NP_478123.1:p.Arg292Lys
ENST00000337432.9:c.875_876delinsAG MANE Select ENSP00000336701.4:p.Arg292Lys
NM_058216.2:c.875_876delinsAG NP_478123.1:p.Arg292Lys
NR_103872.1:n.779_780delinsAG
NR_103872.2:n.750_751delinsAG
ENST00000337432.8:c.875_876delinsAG ENSP00000336701.4:p.Arg292Lys
ENST00000413590.5:c.513_514delinsAG
ENST00000461271.6:c.524_525delinsAG ENSP00000464056.2:p.Arg175Lys
ENST00000475762.5:c.*1541-3257_*1541-3256delinsAG ENSP00000432421.1:n.*1541-3257_*1541-3256delinsAG
ENST00000482007.5:c.*303_*304delinsAG ENSP00000433332.1:n.*303_*304delinsAG
ENST00000487525.5:c.*448_*449delinsAG ENSP00000431637.1:n.*448_*449delinsAG
ENST00000578151.1:n.210_211delinsAG
ENST00000581221.5:n.390_391delinsAG
ENST00000583539.5:c.875_876delinsAG ENSP00000463121.1:p.Arg292Lys
ENST00000584617.5:c.597_598delinsAG
ENST00000584804.1:c.170_171delinsAG ENSP00000463658.1:p.Arg57Lys
ENST00000697678.1:n.777_778delinsAG
ENST00000697679.1:n.1949_1950delinsAG
ENST00000697680.1:c.*1839_*1840delinsAG ENSP00000513392.1:n.*1839_*1840delinsAG
ENST00000697681.1:c.*2036_*2037delinsAG ENSP00000513393.1:n.*2036_*2037delinsAG
ENST00000697683.1:c.*1739_*1740delinsAG ENSP00000513395.1:n.*1739_*1740delinsAG
ENST00000697684.1:n.935_936delinsAG
ENST00000697685.1:c.*1572_*1573delinsAG ENSP00000513396.1:n.*1572_*1573delinsAG
ENST00000697686.1:c.524_525delinsAG ENSP00000513397.1:p.Arg175Lys
ENST00000697687.1:n.754_755delinsAG
ENST00000697688.1:n.921_922delinsAG
ENST00000697689.1:c.*1411_*1412delinsAG ENSP00000513398.1:n.*1411_*1412delinsAG
ENST00000697690.1:c.875_876delinsAG ENSP00000513399.1:p.Arg292Lys
ENST00000697691.1:c.*847_*848delinsAG ENSP00000513400.1:n.*847_*848delinsAG
ENST00000697692.1:c.*887_*888delinsAG ENSP00000513401.1:n.*887_*888delinsAG
ENST00000697694.1:c.524_525delinsAG ENSP00000513402.1:p.Arg175Lys
ENST00000697695.1:n.1482_1483delinsAG
XM_006722001.2:c.875_876delinsAG XP_006722064.1:p.Arg292Lys
XM_006722001.4:c.875_876delinsAG XP_006722064.1:p.Arg292Lys
XM_006722002.2:c.875_876delinsAG XP_006722065.1:p.Arg292Lys
XM_006722002.4:c.875_876delinsAG XP_006722065.1:p.Arg292Lys
XM_006722004.2:c.524_525delinsAG XP_006722067.1:p.Arg175Lys
XM_006722004.3:c.524_525delinsAG XP_006722067.1:p.Arg175Lys
XM_006722005.2:c.524_525delinsAG XP_006722068.1:p.Arg175Lys
XM_006722005.3:c.524_525delinsAG XP_006722068.1:p.Arg175Lys
XM_011525092.1:c.524_525delinsAG XP_011523394.1:p.Arg175Lys
XM_011525092.2:c.524_525delinsAG XP_011523394.1:p.Arg175Lys
XM_011525093.1:c.524_525delinsAG XP_011523395.1:p.Arg175Lys
XM_011525093.2:c.524_525delinsAG XP_011523395.1:p.Arg175Lys
XM_011525094.1:c.524_525delinsAG XP_011523396.1:p.Arg175Lys
XM_011525094.2:c.524_525delinsAG XP_011523396.1:p.Arg175Lys
XM_017024914.1:c.524_525delinsAG XP_016880403.1:p.Arg175Lys
XM_017024915.1:c.524_525delinsAG XP_016880404.1:p.Arg175Lys
XM_017024916.1:c.524_525delinsAG XP_016880405.1:p.Arg175Lys
XM_017024917.1:c.524_525delinsAG XP_016880406.1:p.Arg175Lys
XM_017024918.2:c.524_525delinsAG XP_016880407.1:p.Arg175Lys
XM_017024919.1:c.524_525delinsAG XP_016880408.1:p.Arg175Lys
XR_934513.1:n.1093_1094delinsAG
XR_934513.3:n.1524_1525delinsAG
XR_934514.1:n.1093_1094delinsAG
XR_934514.3:n.1524_1525delinsAG