Canonical Allele Identifier: CA3057242771
Community Standard Title: NM_058216.3(RAD51C):c.678_679delinsCT (p.Pro227Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703302_58703303delinsCT , CM000679.2:g.58703302_58703303delinsCT GRCh38
NC_000017.10:g.56780663_56780664delinsCT , CM000679.1:g.56780663_56780664delinsCT GRCh37
NC_000017.9:g.54135662_54135663delinsCT NCBI36
NG_023199.1:g.15701_15702delinsCT , LRG_314:g.15701_15702delinsCT

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.678_679delinsCT MANE Select NP_478123.1:p.Pro227Ser
ENST00000337432.9:c.678_679delinsCT MANE Select ENSP00000336701.4:p.Pro227Ser
NM_058216.2:c.678_679delinsCT NP_478123.1:p.Pro227Ser
NR_103872.1:n.582_583delinsCT
NR_103872.2:n.553_554delinsCT
ENST00000337432.8:c.678_679delinsCT ENSP00000336701.4:p.Pro227Ser
ENST00000413590.5:c.316_317delinsCT
ENST00000425173.5:c.474_475delinsCT ENSP00000407282.1:p.Pro159Ser
ENST00000461271.5:c.327_328delinsCT ENSP00000464056.1:p.Pro110Ser
ENST00000461271.6:c.327_328delinsCT ENSP00000464056.2:p.Pro110Ser
ENST00000475762.5:c.*1381_*1382delinsCT ENSP00000432421.1:n.*1381_*1382delinsCT
ENST00000482007.5:c.*106_*107delinsCT ENSP00000433332.1:n.*106_*107delinsCT
ENST00000487525.5:c.*106_*107delinsCT ENSP00000431637.1:n.*106_*107delinsCT
ENST00000487921.5:n.590_591delinsCT
ENST00000583539.5:c.678_679delinsCT ENSP00000463121.1:p.Pro227Ser
ENST00000584617.5:c.400_401delinsCT
ENST00000697677.1:n.1759_1760delinsCT
ENST00000697678.1:n.580_581delinsCT
ENST00000697679.1:n.1752_1753delinsCT
ENST00000697680.1:c.*1542_*1543delinsCT ENSP00000513392.1:n.*1542_*1543delinsCT
ENST00000697681.1:c.*1694_*1695delinsCT ENSP00000513393.1:n.*1694_*1695delinsCT
ENST00000697683.1:c.*1542_*1543delinsCT ENSP00000513395.1:n.*1542_*1543delinsCT
ENST00000697684.1:n.738_739delinsCT
ENST00000697685.1:c.*1375_*1376delinsCT ENSP00000513396.1:n.*1375_*1376delinsCT
ENST00000697686.1:c.327_328delinsCT ENSP00000513397.1:p.Pro110Ser
ENST00000697687.1:n.557_558delinsCT
ENST00000697688.1:n.724_725delinsCT
ENST00000697689.1:c.*1214_*1215delinsCT ENSP00000513398.1:n.*1214_*1215delinsCT
ENST00000697690.1:c.678_679delinsCT ENSP00000513399.1:p.Pro227Ser
ENST00000697691.1:c.*650_*651delinsCT ENSP00000513400.1:n.*650_*651delinsCT
ENST00000697692.1:c.*690_*691delinsCT ENSP00000513401.1:n.*690_*691delinsCT
ENST00000697694.1:c.327_328delinsCT ENSP00000513402.1:p.Pro110Ser
ENST00000697695.1:n.1285_1286delinsCT
XM_006722001.2:c.678_679delinsCT XP_006722064.1:p.Pro227Ser
XM_006722001.4:c.678_679delinsCT XP_006722064.1:p.Pro227Ser
XM_006722002.2:c.678_679delinsCT XP_006722065.1:p.Pro227Ser
XM_006722002.4:c.678_679delinsCT XP_006722065.1:p.Pro227Ser
XM_006722004.2:c.327_328delinsCT XP_006722067.1:p.Pro110Ser
XM_006722004.3:c.327_328delinsCT XP_006722067.1:p.Pro110Ser
XM_006722005.2:c.327_328delinsCT XP_006722068.1:p.Pro110Ser
XM_006722005.3:c.327_328delinsCT XP_006722068.1:p.Pro110Ser
XM_011525092.1:c.327_328delinsCT XP_011523394.1:p.Pro110Ser
XM_011525092.2:c.327_328delinsCT XP_011523394.1:p.Pro110Ser
XM_011525093.1:c.327_328delinsCT XP_011523395.1:p.Pro110Ser
XM_011525093.2:c.327_328delinsCT XP_011523395.1:p.Pro110Ser
XM_011525094.1:c.327_328delinsCT XP_011523396.1:p.Pro110Ser
XM_011525094.2:c.327_328delinsCT XP_011523396.1:p.Pro110Ser
XM_017024914.1:c.327_328delinsCT XP_016880403.1:p.Pro110Ser
XM_017024915.1:c.327_328delinsCT XP_016880404.1:p.Pro110Ser
XM_017024916.1:c.327_328delinsCT XP_016880405.1:p.Pro110Ser
XM_017024917.1:c.327_328delinsCT XP_016880406.1:p.Pro110Ser
XM_017024918.2:c.327_328delinsCT XP_016880407.1:p.Pro110Ser
XM_017024919.1:c.327_328delinsCT XP_016880408.1:p.Pro110Ser
XR_934513.1:n.751_752delinsCT
XR_934513.3:n.1182_1183delinsCT
XR_934514.1:n.751_752delinsCT
XR_934514.3:n.1182_1183delinsCT