Canonical Allele Identifier: CA3261180360
Community Standard Title: NM_058216.3(RAD51C):c.691_693delinsCTG (p.Ser231Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703315_58703317delinsCTG , CM000679.2:g.58703315_58703317delinsCTG GRCh38
NC_000017.10:g.56780676_56780678delinsCTG , CM000679.1:g.56780676_56780678delinsCTG GRCh37
NC_000017.9:g.54135675_54135677delinsCTG NCBI36
NG_023199.1:g.15714_15716delinsCTG , LRG_314:g.15714_15716delinsCTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.691_693delinsCTG MANE Select NP_478123.1:p.Ser231Leu
ENST00000337432.9:c.691_693delinsCTG MANE Select ENSP00000336701.4:p.Ser231Leu
NM_058216.2:c.691_693delinsCTG NP_478123.1:p.Ser231Leu
NR_103872.1:n.595_597delinsCTG
NR_103872.2:n.566_568delinsCTG
ENST00000337432.8:c.691_693delinsCTG ENSP00000336701.4:p.Ser231Leu
ENST00000413590.5:c.329_331delinsCTG
ENST00000425173.5:c.487_489delinsCTG ENSP00000407282.1:p.Ser163Leu
ENST00000461271.5:c.340_342delinsCTG ENSP00000464056.1:p.Ser114Leu
ENST00000461271.6:c.340_342delinsCTG ENSP00000464056.2:p.Ser114Leu
ENST00000475762.5:c.*1394_*1396delinsCTG ENSP00000432421.1:n.*1394_*1396delinsCTG
ENST00000482007.5:c.*119_*121delinsCTG ENSP00000433332.1:n.*119_*121delinsCTG
ENST00000487525.5:c.*119_*121delinsCTG ENSP00000431637.1:n.*119_*121delinsCTG
ENST00000487921.5:n.603_605delinsCTG
ENST00000583539.5:c.691_693delinsCTG ENSP00000463121.1:p.Ser231Leu
ENST00000584617.5:c.413_415delinsCTG
ENST00000697677.1:n.1772_1774delinsCTG
ENST00000697678.1:n.593_595delinsCTG
ENST00000697679.1:n.1765_1767delinsCTG
ENST00000697680.1:c.*1555_*1557delinsCTG ENSP00000513392.1:n.*1555_*1557delinsCTG
ENST00000697681.1:c.*1707_*1709delinsCTG ENSP00000513393.1:n.*1707_*1709delinsCTG
ENST00000697683.1:c.*1555_*1557delinsCTG ENSP00000513395.1:n.*1555_*1557delinsCTG
ENST00000697684.1:n.751_753delinsCTG
ENST00000697685.1:c.*1388_*1390delinsCTG ENSP00000513396.1:n.*1388_*1390delinsCTG
ENST00000697686.1:c.340_342delinsCTG ENSP00000513397.1:p.Ser114Leu
ENST00000697687.1:n.570_572delinsCTG
ENST00000697688.1:n.737_739delinsCTG
ENST00000697689.1:c.*1227_*1229delinsCTG ENSP00000513398.1:n.*1227_*1229delinsCTG
ENST00000697690.1:c.691_693delinsCTG ENSP00000513399.1:p.Ser231Leu
ENST00000697691.1:c.*663_*665delinsCTG ENSP00000513400.1:n.*663_*665delinsCTG
ENST00000697692.1:c.*703_*705delinsCTG ENSP00000513401.1:n.*703_*705delinsCTG
ENST00000697694.1:c.340_342delinsCTG ENSP00000513402.1:p.Ser114Leu
ENST00000697695.1:n.1298_1300delinsCTG
XM_006722001.2:c.691_693delinsCTG XP_006722064.1:p.Ser231Leu
XM_006722001.4:c.691_693delinsCTG XP_006722064.1:p.Ser231Leu
XM_006722002.2:c.691_693delinsCTG XP_006722065.1:p.Ser231Leu
XM_006722002.4:c.691_693delinsCTG XP_006722065.1:p.Ser231Leu
XM_006722004.2:c.340_342delinsCTG XP_006722067.1:p.Ser114Leu
XM_006722004.3:c.340_342delinsCTG XP_006722067.1:p.Ser114Leu
XM_006722005.2:c.340_342delinsCTG XP_006722068.1:p.Ser114Leu
XM_006722005.3:c.340_342delinsCTG XP_006722068.1:p.Ser114Leu
XM_011525092.1:c.340_342delinsCTG XP_011523394.1:p.Ser114Leu
XM_011525092.2:c.340_342delinsCTG XP_011523394.1:p.Ser114Leu
XM_011525093.1:c.340_342delinsCTG XP_011523395.1:p.Ser114Leu
XM_011525093.2:c.340_342delinsCTG XP_011523395.1:p.Ser114Leu
XM_011525094.1:c.340_342delinsCTG XP_011523396.1:p.Ser114Leu
XM_011525094.2:c.340_342delinsCTG XP_011523396.1:p.Ser114Leu
XM_017024914.1:c.340_342delinsCTG XP_016880403.1:p.Ser114Leu
XM_017024915.1:c.340_342delinsCTG XP_016880404.1:p.Ser114Leu
XM_017024916.1:c.340_342delinsCTG XP_016880405.1:p.Ser114Leu
XM_017024917.1:c.340_342delinsCTG XP_016880406.1:p.Ser114Leu
XM_017024918.2:c.340_342delinsCTG XP_016880407.1:p.Ser114Leu
XM_017024919.1:c.340_342delinsCTG XP_016880408.1:p.Ser114Leu
XR_934513.1:n.764_766delinsCTG
XR_934513.3:n.1195_1197delinsCTG
XR_934514.1:n.764_766delinsCTG
XR_934514.3:n.1195_1197delinsCTG