Canonical Allele Identifier: CA3261180252
Community Standard Title: NM_058216.3(RAD51C):c.1066_1068delinsCTG (p.Ser356Leu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734157_58734159delinsCTG , CM000679.2:g.58734157_58734159delinsCTG GRCh38
NC_000017.10:g.56811518_56811520delinsCTG , CM000679.1:g.56811518_56811520delinsCTG GRCh37
NC_000017.9:g.54166517_54166519delinsCTG NCBI36
NG_023199.1:g.46556_46558delinsCTG , LRG_314:g.46556_46558delinsCTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1066_1068delinsCTG MANE Select NP_478123.1:p.Ser356Leu
ENST00000337432.9:c.1066_1068delinsCTG MANE Select ENSP00000336701.4:p.Ser356Leu
NM_058216.2:c.1066_1068delinsCTG NP_478123.1:p.Ser356Leu
NR_103872.1:n.970_972delinsCTG
NR_103872.2:n.941_943delinsCTG
ENST00000337432.8:c.1066_1068delinsCTG ENSP00000336701.4:p.Ser356Leu
ENST00000413590.5:c.707_709delinsCTG
ENST00000461271.6:c.*1598_*1600delinsCTG ENSP00000464056.2:n.*1598_*1600delinsCTG
ENST00000461706.1:n.253_255delinsCTG
ENST00000475762.5:c.*1702_*1704delinsCTG ENSP00000432421.1:n.*1702_*1704delinsCTG
ENST00000482007.5:c.*494_*496delinsCTG ENSP00000433332.1:n.*494_*496delinsCTG
ENST00000487525.5:c.*642_*644delinsCTG ENSP00000431637.1:n.*642_*644delinsCTG
ENST00000578151.1:n.279_281delinsCTG
ENST00000581221.5:n.581_583delinsCTG
ENST00000584804.1:c.300_302delinsCTG ENSP00000463658.1:p.His101Cys
ENST00000697680.1:c.*2030_*2032delinsCTG ENSP00000513392.1:n.*2030_*2032delinsCTG
ENST00000697681.1:c.*2227_*2229delinsCTG ENSP00000513393.1:n.*2227_*2229delinsCTG
ENST00000697683.1:c.*2002_*2004delinsCTG ENSP00000513395.1:n.*2002_*2004delinsCTG
ENST00000697685.1:c.*1763_*1765delinsCTG ENSP00000513396.1:n.*1763_*1765delinsCTG
ENST00000697686.1:c.837_839delinsCTG ENSP00000513397.1:p.His280Cys
ENST00000697689.1:c.*1480_*1482delinsCTG ENSP00000513398.1:n.*1480_*1482delinsCTG
ENST00000697690.1:c.*26_*28delinsCTG ENSP00000513399.1:n.*26_*28delinsCTG
ENST00000697691.1:c.*1038_*1040delinsCTG ENSP00000513400.1:n.*1038_*1040delinsCTG
ENST00000697692.1:c.*1078_*1080delinsCTG ENSP00000513401.1:n.*1078_*1080delinsCTG
ENST00000697694.1:c.715_717delinsCTG ENSP00000513402.1:p.Ser239Leu
ENST00000697695.1:n.1673_1675delinsCTG
XM_006722001.2:c.1069_1071delinsCTG XP_006722064.1:p.Ser357Leu
XM_006722001.4:c.1069_1071delinsCTG XP_006722064.1:p.Ser357Leu
XM_006722002.2:c.1005_1007delinsCTG XP_006722065.1:p.His336Cys
XM_006722002.4:c.1005_1007delinsCTG XP_006722065.1:p.His336Cys
XM_006722004.2:c.718_720delinsCTG XP_006722067.1:p.Ser240Leu
XM_006722004.3:c.718_720delinsCTG XP_006722067.1:p.Ser240Leu
XM_006722005.2:c.718_720delinsCTG XP_006722068.1:p.Ser240Leu
XM_006722005.3:c.718_720delinsCTG XP_006722068.1:p.Ser240Leu
XM_011525092.1:c.718_720delinsCTG XP_011523394.1:p.Ser240Leu
XM_011525092.2:c.718_720delinsCTG XP_011523394.1:p.Ser240Leu
XM_011525093.1:c.718_720delinsCTG XP_011523395.1:p.Ser240Leu
XM_011525093.2:c.718_720delinsCTG XP_011523395.1:p.Ser240Leu
XM_011525094.1:c.718_720delinsCTG XP_011523396.1:p.Ser240Leu
XM_011525094.2:c.718_720delinsCTG XP_011523396.1:p.Ser240Leu
XM_017024914.1:c.715_717delinsCTG XP_016880403.1:p.Ser239Leu
XM_017024915.1:c.715_717delinsCTG XP_016880404.1:p.Ser239Leu
XM_017024916.1:c.715_717delinsCTG XP_016880405.1:p.Ser239Leu
XM_017024917.1:c.715_717delinsCTG XP_016880406.1:p.Ser239Leu
XM_017024918.2:c.715_717delinsCTG XP_016880407.1:p.Ser239Leu
XM_017024919.1:c.654_656delinsCTG XP_016880408.1:p.His219Cys
XR_934513.1:n.1284_1286delinsCTG
XR_934513.3:n.1715_1717delinsCTG
XR_934514.1:n.1287_1289delinsCTG
XR_934514.3:n.1718_1720delinsCTG
XR_934886.1:n.149+3912_149+3914delinsCAG
XR_934886.2:n.149+3912_149+3914delinsCAG