Canonical Allele Identifier: CA3261179229
Community Standard Title: NM_058216.3(RAD51C):c.617_618delinsAC (p.Ser206Tyr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703241_58703242delinsAC , CM000679.2:g.58703241_58703242delinsAC GRCh38
NC_000017.10:g.56780602_56780603delinsAC , CM000679.1:g.56780602_56780603delinsAC GRCh37
NC_000017.9:g.54135601_54135602delinsAC NCBI36
NG_023199.1:g.15640_15641delinsAC , LRG_314:g.15640_15641delinsAC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.617_618delinsAC MANE Select NP_478123.1:p.Ser206Tyr
ENST00000337432.9:c.617_618delinsAC MANE Select ENSP00000336701.4:p.Ser206Tyr
NM_058216.2:c.617_618delinsAC NP_478123.1:p.Ser206Tyr
NR_103872.1:n.521_522delinsAC
NR_103872.2:n.492_493delinsAC
ENST00000337432.8:c.617_618delinsAC ENSP00000336701.4:p.Ser206Tyr
ENST00000413590.5:c.255_256delinsAC
ENST00000425173.5:c.413_414delinsAC ENSP00000407282.1:p.Ser138Tyr
ENST00000461271.5:c.266_267delinsAC ENSP00000464056.1:p.Ser89Tyr
ENST00000461271.6:c.266_267delinsAC ENSP00000464056.2:p.Ser89Tyr
ENST00000475762.5:c.*1320_*1321delinsAC ENSP00000432421.1:n.*1320_*1321delinsAC
ENST00000482007.5:c.*45_*46delinsAC ENSP00000433332.1:n.*45_*46delinsAC
ENST00000487525.5:c.*45_*46delinsAC ENSP00000431637.1:n.*45_*46delinsAC
ENST00000487921.5:n.529_530delinsAC
ENST00000583539.5:c.617_618delinsAC ENSP00000463121.1:p.Ser206Tyr
ENST00000584617.5:c.339_340delinsAC
ENST00000697677.1:n.1698_1699delinsAC
ENST00000697678.1:n.519_520delinsAC
ENST00000697679.1:n.1691_1692delinsAC
ENST00000697680.1:c.*1481_*1482delinsAC ENSP00000513392.1:n.*1481_*1482delinsAC
ENST00000697681.1:c.*1633_*1634delinsAC ENSP00000513393.1:n.*1633_*1634delinsAC
ENST00000697683.1:c.*1481_*1482delinsAC ENSP00000513395.1:n.*1481_*1482delinsAC
ENST00000697684.1:n.677_678delinsAC
ENST00000697685.1:c.*1314_*1315delinsAC ENSP00000513396.1:n.*1314_*1315delinsAC
ENST00000697686.1:c.266_267delinsAC ENSP00000513397.1:p.Ser89Tyr
ENST00000697687.1:n.496_497delinsAC
ENST00000697688.1:n.663_664delinsAC
ENST00000697689.1:c.*1153_*1154delinsAC ENSP00000513398.1:n.*1153_*1154delinsAC
ENST00000697690.1:c.617_618delinsAC ENSP00000513399.1:p.Ser206Tyr
ENST00000697691.1:c.*589_*590delinsAC ENSP00000513400.1:n.*589_*590delinsAC
ENST00000697692.1:c.*629_*630delinsAC ENSP00000513401.1:n.*629_*630delinsAC
ENST00000697694.1:c.266_267delinsAC ENSP00000513402.1:p.Ser89Tyr
ENST00000697695.1:n.1224_1225delinsAC
XM_006722001.2:c.617_618delinsAC XP_006722064.1:p.Ser206Tyr
XM_006722001.4:c.617_618delinsAC XP_006722064.1:p.Ser206Tyr
XM_006722002.2:c.617_618delinsAC XP_006722065.1:p.Ser206Tyr
XM_006722002.4:c.617_618delinsAC XP_006722065.1:p.Ser206Tyr
XM_006722004.2:c.266_267delinsAC XP_006722067.1:p.Ser89Tyr
XM_006722004.3:c.266_267delinsAC XP_006722067.1:p.Ser89Tyr
XM_006722005.2:c.266_267delinsAC XP_006722068.1:p.Ser89Tyr
XM_006722005.3:c.266_267delinsAC XP_006722068.1:p.Ser89Tyr
XM_011525092.1:c.266_267delinsAC XP_011523394.1:p.Ser89Tyr
XM_011525092.2:c.266_267delinsAC XP_011523394.1:p.Ser89Tyr
XM_011525093.1:c.266_267delinsAC XP_011523395.1:p.Ser89Tyr
XM_011525093.2:c.266_267delinsAC XP_011523395.1:p.Ser89Tyr
XM_011525094.1:c.266_267delinsAC XP_011523396.1:p.Ser89Tyr
XM_011525094.2:c.266_267delinsAC XP_011523396.1:p.Ser89Tyr
XM_017024914.1:c.266_267delinsAC XP_016880403.1:p.Ser89Tyr
XM_017024915.1:c.266_267delinsAC XP_016880404.1:p.Ser89Tyr
XM_017024916.1:c.266_267delinsAC XP_016880405.1:p.Ser89Tyr
XM_017024917.1:c.266_267delinsAC XP_016880406.1:p.Ser89Tyr
XM_017024918.2:c.266_267delinsAC XP_016880407.1:p.Ser89Tyr
XM_017024919.1:c.266_267delinsAC XP_016880408.1:p.Ser89Tyr
XR_934513.1:n.690_691delinsAC
XR_934513.3:n.1121_1122delinsAC
XR_934514.1:n.690_691delinsAC
XR_934514.3:n.1121_1122delinsAC