Canonical Allele Identifier: CA3261179847
Community Standard Title: NM_058216.3(RAD51C):c.935_936delinsAA (p.Arg312Gln)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724070_58724071delinsAA , CM000679.2:g.58724070_58724071delinsAA GRCh38
NC_000017.10:g.56801431_56801432delinsAA , CM000679.1:g.56801431_56801432delinsAA GRCh37
NC_000017.9:g.54156430_54156431delinsAA NCBI36
NG_023199.1:g.36469_36470delinsAA , LRG_314:g.36469_36470delinsAA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.935_936delinsAA MANE Select NP_478123.1:p.Arg312Gln
ENST00000337432.9:c.935_936delinsAA MANE Select ENSP00000336701.4:p.Arg312Gln
NM_058216.2:c.935_936delinsAA NP_478123.1:p.Arg312Gln
NR_103872.1:n.839_840delinsAA
NR_103872.2:n.810_811delinsAA
ENST00000337432.8:c.935_936delinsAA ENSP00000336701.4:p.Arg312Gln
ENST00000413590.5:c.573_574delinsAA
ENST00000461271.6:c.584_585delinsAA ENSP00000464056.2:p.Arg195Gln
ENST00000475762.5:c.*1571_*1572delinsAA ENSP00000432421.1:n.*1571_*1572delinsAA
ENST00000482007.5:c.*363_*364delinsAA ENSP00000433332.1:n.*363_*364delinsAA
ENST00000487525.5:c.*508_*509delinsAA ENSP00000431637.1:n.*508_*509delinsAA
ENST00000578151.1:n.239+3258_239+3259delinsAA
ENST00000581221.5:n.450_451delinsAA
ENST00000583539.5:c.935_936delinsAA ENSP00000463121.1:p.Arg312Gln
ENST00000584617.5:c.657_658delinsAA
ENST00000584804.1:c.199+3258_199+3259delinsAA ENSP00000463658.1:n.199+3258_199+3259delinsAA
ENST00000697680.1:c.*1899_*1900delinsAA ENSP00000513392.1:n.*1899_*1900delinsAA
ENST00000697681.1:c.*2096_*2097delinsAA ENSP00000513393.1:n.*2096_*2097delinsAA
ENST00000697683.1:c.*1799_*1800delinsAA ENSP00000513395.1:n.*1799_*1800delinsAA
ENST00000697684.1:n.995_996delinsAA
ENST00000697685.1:c.*1632_*1633delinsAA ENSP00000513396.1:n.*1632_*1633delinsAA
ENST00000697686.1:c.584_585delinsAA ENSP00000513397.1:p.Arg195Gln
ENST00000697687.1:n.814_815delinsAA
ENST00000697688.1:n.981_982delinsAA
ENST00000697689.1:c.*1440+3258_*1440+3259delinsAA ENSP00000513398.1:n.*1440+3258_*1440+3259delinsAA
ENST00000697690.1:c.904+3258_904+3259delinsAA ENSP00000513399.1:n.904+3258_904+3259delinsAA
ENST00000697691.1:c.*907_*908delinsAA ENSP00000513400.1:n.*907_*908delinsAA
ENST00000697692.1:c.*947_*948delinsAA ENSP00000513401.1:n.*947_*948delinsAA
ENST00000697694.1:c.584_585delinsAA ENSP00000513402.1:p.Arg195Gln
ENST00000697695.1:n.1542_1543delinsAA
XM_006722001.2:c.935_936delinsAA XP_006722064.1:p.Arg312Gln
XM_006722001.4:c.935_936delinsAA XP_006722064.1:p.Arg312Gln
XM_006722002.2:c.904+3258_904+3259delinsAA XP_006722065.1:n.904+3258_904+3259delinsAA
XM_006722002.4:c.904+3258_904+3259delinsAA XP_006722065.1:n.904+3258_904+3259delinsAA
XM_006722004.2:c.584_585delinsAA XP_006722067.1:p.Arg195Gln
XM_006722004.3:c.584_585delinsAA XP_006722067.1:p.Arg195Gln
XM_006722005.2:c.584_585delinsAA XP_006722068.1:p.Arg195Gln
XM_006722005.3:c.584_585delinsAA XP_006722068.1:p.Arg195Gln
XM_011525092.1:c.584_585delinsAA XP_011523394.1:p.Arg195Gln
XM_011525092.2:c.584_585delinsAA XP_011523394.1:p.Arg195Gln
XM_011525093.1:c.584_585delinsAA XP_011523395.1:p.Arg195Gln
XM_011525093.2:c.584_585delinsAA XP_011523395.1:p.Arg195Gln
XM_011525094.1:c.584_585delinsAA XP_011523396.1:p.Arg195Gln
XM_011525094.2:c.584_585delinsAA XP_011523396.1:p.Arg195Gln
XM_017024914.1:c.584_585delinsAA XP_016880403.1:p.Arg195Gln
XM_017024915.1:c.584_585delinsAA XP_016880404.1:p.Arg195Gln
XM_017024916.1:c.584_585delinsAA XP_016880405.1:p.Arg195Gln
XM_017024917.1:c.584_585delinsAA XP_016880406.1:p.Arg195Gln
XM_017024918.2:c.584_585delinsAA XP_016880407.1:p.Arg195Gln
XM_017024919.1:c.553+3258_553+3259delinsAA XP_016880408.1:n.553+3258_553+3259delinsAA
XR_934513.1:n.1153_1154delinsAA
XR_934513.3:n.1584_1585delinsAA
XR_934514.1:n.1153_1154delinsAA
XR_934514.3:n.1584_1585delinsAA