Canonical Allele Identifier: CA3261180114
Community Standard Title: NM_058216.3(RAD51C):c.955_957delinsGGC (p.Arg319Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724090_58724092delinsGGC , CM000679.2:g.58724090_58724092delinsGGC GRCh38
NC_000017.10:g.56801451_56801453delinsGGC , CM000679.1:g.56801451_56801453delinsGGC GRCh37
NC_000017.9:g.54156450_54156452delinsGGC NCBI36
NG_023199.1:g.36489_36491delinsGGC , LRG_314:g.36489_36491delinsGGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.955_957delinsGGC MANE Select NP_478123.1:p.Arg319Gly
ENST00000337432.9:c.955_957delinsGGC MANE Select ENSP00000336701.4:p.Arg319Gly
NM_058216.2:c.955_957delinsGGC NP_478123.1:p.Arg319Gly
NR_103872.1:n.859_861delinsGGC
NR_103872.2:n.830_832delinsGGC
ENST00000337432.8:c.955_957delinsGGC ENSP00000336701.4:p.Arg319Gly
ENST00000413590.5:c.593_595delinsGGC
ENST00000461271.6:c.604_606delinsGGC ENSP00000464056.2:p.Arg202Gly
ENST00000475762.5:c.*1591_*1593delinsGGC ENSP00000432421.1:n.*1591_*1593delinsGGC
ENST00000482007.5:c.*383_*385delinsGGC ENSP00000433332.1:n.*383_*385delinsGGC
ENST00000487525.5:c.*528_*530delinsGGC ENSP00000431637.1:n.*528_*530delinsGGC
ENST00000578151.1:n.239+3278_239+3280delinsGGC
ENST00000581221.5:n.470_472delinsGGC
ENST00000583539.5:c.955_957delinsGGC ENSP00000463121.1:p.Arg319Gly
ENST00000584617.5:c.677_679delinsGGC
ENST00000584804.1:c.199+3278_199+3280delinsGGC ENSP00000463658.1:n.199+3278_199+3280delinsGGC
ENST00000697680.1:c.*1919_*1921delinsGGC ENSP00000513392.1:n.*1919_*1921delinsGGC
ENST00000697681.1:c.*2116_*2118delinsGGC ENSP00000513393.1:n.*2116_*2118delinsGGC
ENST00000697683.1:c.*1819_*1821delinsGGC ENSP00000513395.1:n.*1819_*1821delinsGGC
ENST00000697684.1:n.1015_1017delinsGGC
ENST00000697685.1:c.*1652_*1654delinsGGC ENSP00000513396.1:n.*1652_*1654delinsGGC
ENST00000697686.1:c.604_606delinsGGC ENSP00000513397.1:p.Arg202Gly
ENST00000697687.1:n.834_836delinsGGC
ENST00000697688.1:n.1001_1003delinsGGC
ENST00000697689.1:c.*1440+3278_*1440+3280delinsGGC ENSP00000513398.1:n.*1440+3278_*1440+3280delinsGGC
ENST00000697690.1:c.904+3278_904+3280delinsGGC ENSP00000513399.1:n.904+3278_904+3280delinsGGC
ENST00000697691.1:c.*927_*929delinsGGC ENSP00000513400.1:n.*927_*929delinsGGC
ENST00000697692.1:c.*967_*969delinsGGC ENSP00000513401.1:n.*967_*969delinsGGC
ENST00000697694.1:c.604_606delinsGGC ENSP00000513402.1:p.Arg202Gly
ENST00000697695.1:n.1562_1564delinsGGC
XM_006722001.2:c.955_957delinsGGC XP_006722064.1:p.Arg319Gly
XM_006722001.4:c.955_957delinsGGC XP_006722064.1:p.Arg319Gly
XM_006722002.2:c.904+3278_904+3280delinsGGC XP_006722065.1:n.904+3278_904+3280delinsGGC
XM_006722002.4:c.904+3278_904+3280delinsGGC XP_006722065.1:n.904+3278_904+3280delinsGGC
XM_006722004.2:c.604_606delinsGGC XP_006722067.1:p.Arg202Gly
XM_006722004.3:c.604_606delinsGGC XP_006722067.1:p.Arg202Gly
XM_006722005.2:c.604_606delinsGGC XP_006722068.1:p.Arg202Gly
XM_006722005.3:c.604_606delinsGGC XP_006722068.1:p.Arg202Gly
XM_011525092.1:c.604_606delinsGGC XP_011523394.1:p.Arg202Gly
XM_011525092.2:c.604_606delinsGGC XP_011523394.1:p.Arg202Gly
XM_011525093.1:c.604_606delinsGGC XP_011523395.1:p.Arg202Gly
XM_011525093.2:c.604_606delinsGGC XP_011523395.1:p.Arg202Gly
XM_011525094.1:c.604_606delinsGGC XP_011523396.1:p.Arg202Gly
XM_011525094.2:c.604_606delinsGGC XP_011523396.1:p.Arg202Gly
XM_017024914.1:c.604_606delinsGGC XP_016880403.1:p.Arg202Gly
XM_017024915.1:c.604_606delinsGGC XP_016880404.1:p.Arg202Gly
XM_017024916.1:c.604_606delinsGGC XP_016880405.1:p.Arg202Gly
XM_017024917.1:c.604_606delinsGGC XP_016880406.1:p.Arg202Gly
XM_017024918.2:c.604_606delinsGGC XP_016880407.1:p.Arg202Gly
XM_017024919.1:c.553+3278_553+3280delinsGGC XP_016880408.1:n.553+3278_553+3280delinsGGC
XR_934513.1:n.1173_1175delinsGGC
XR_934513.3:n.1604_1606delinsGGC
XR_934514.1:n.1173_1175delinsGGC
XR_934514.3:n.1604_1606delinsGGC