Canonical Allele Identifier: CA3261179493
Community Standard Title: NM_058216.3(RAD51C):c.1027_1029delinsAGC (p.Pro343Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734118_58734120delinsAGC , CM000679.2:g.58734118_58734120delinsAGC GRCh38
NC_000017.10:g.56811479_56811481delinsAGC , CM000679.1:g.56811479_56811481delinsAGC GRCh37
NC_000017.9:g.54166478_54166480delinsAGC NCBI36
NG_023199.1:g.46517_46519delinsAGC , LRG_314:g.46517_46519delinsAGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1027_1029delinsAGC MANE Select NP_478123.1:p.Pro343Ser
ENST00000337432.9:c.1027_1029delinsAGC MANE Select ENSP00000336701.4:p.Pro343Ser
NM_058216.2:c.1027_1029delinsAGC NP_478123.1:p.Pro343Ser
NR_103872.1:n.931_933delinsAGC
NR_103872.2:n.902_904delinsAGC
ENST00000337432.8:c.1027_1029delinsAGC ENSP00000336701.4:p.Pro343Ser
ENST00000413590.5:c.668_670delinsAGC
ENST00000461271.6:c.*1559_*1561delinsAGC ENSP00000464056.2:n.*1559_*1561delinsAGC
ENST00000461706.1:n.214_216delinsAGC
ENST00000475762.5:c.*1663_*1665delinsAGC ENSP00000432421.1:n.*1663_*1665delinsAGC
ENST00000482007.5:c.*455_*457delinsAGC ENSP00000433332.1:n.*455_*457delinsAGC
ENST00000487525.5:c.*603_*605delinsAGC ENSP00000431637.1:n.*603_*605delinsAGC
ENST00000578151.1:n.240_242delinsAGC
ENST00000581221.5:n.542_544delinsAGC
ENST00000584804.1:c.261_263delinsAGC ENSP00000463658.1:p.Asn87_Leu88delinsLysAla
ENST00000697680.1:c.*1991_*1993delinsAGC ENSP00000513392.1:n.*1991_*1993delinsAGC
ENST00000697681.1:c.*2188_*2190delinsAGC ENSP00000513393.1:n.*2188_*2190delinsAGC
ENST00000697683.1:c.*1963_*1965delinsAGC ENSP00000513395.1:n.*1963_*1965delinsAGC
ENST00000697685.1:c.*1724_*1726delinsAGC ENSP00000513396.1:n.*1724_*1726delinsAGC
ENST00000697686.1:c.798_800delinsAGC ENSP00000513397.1:p.Asn266_Leu267delinsLysAla
ENST00000697689.1:c.*1441_*1443delinsAGC ENSP00000513398.1:n.*1441_*1443delinsAGC
ENST00000697690.1:c.905_907delinsAGC ENSP00000513399.1:p.Ala302_Ser303delinsGluPro
ENST00000697691.1:c.*999_*1001delinsAGC ENSP00000513400.1:n.*999_*1001delinsAGC
ENST00000697692.1:c.*1039_*1041delinsAGC ENSP00000513401.1:n.*1039_*1041delinsAGC
ENST00000697694.1:c.676_678delinsAGC ENSP00000513402.1:p.Pro226Ser
ENST00000697695.1:n.1634_1636delinsAGC
XM_006722001.2:c.1030_1032delinsAGC XP_006722064.1:p.Pro344Ser
XM_006722001.4:c.1030_1032delinsAGC XP_006722064.1:p.Pro344Ser
XM_006722002.2:c.966_968delinsAGC XP_006722065.1:p.Asn322_Leu323delinsLysAla
XM_006722002.4:c.966_968delinsAGC XP_006722065.1:p.Asn322_Leu323delinsLysAla
XM_006722004.2:c.679_681delinsAGC XP_006722067.1:p.Pro227Ser
XM_006722004.3:c.679_681delinsAGC XP_006722067.1:p.Pro227Ser
XM_006722005.2:c.679_681delinsAGC XP_006722068.1:p.Pro227Ser
XM_006722005.3:c.679_681delinsAGC XP_006722068.1:p.Pro227Ser
XM_011525092.1:c.679_681delinsAGC XP_011523394.1:p.Pro227Ser
XM_011525092.2:c.679_681delinsAGC XP_011523394.1:p.Pro227Ser
XM_011525093.1:c.679_681delinsAGC XP_011523395.1:p.Pro227Ser
XM_011525093.2:c.679_681delinsAGC XP_011523395.1:p.Pro227Ser
XM_011525094.1:c.679_681delinsAGC XP_011523396.1:p.Pro227Ser
XM_011525094.2:c.679_681delinsAGC XP_011523396.1:p.Pro227Ser
XM_017024914.1:c.676_678delinsAGC XP_016880403.1:p.Pro226Ser
XM_017024915.1:c.676_678delinsAGC XP_016880404.1:p.Pro226Ser
XM_017024916.1:c.676_678delinsAGC XP_016880405.1:p.Pro226Ser
XM_017024917.1:c.676_678delinsAGC XP_016880406.1:p.Pro226Ser
XM_017024918.2:c.676_678delinsAGC XP_016880407.1:p.Pro226Ser
XM_017024919.1:c.615_617delinsAGC XP_016880408.1:p.Asn205_Leu206delinsLysAla
XR_934513.1:n.1245_1247delinsAGC
XR_934513.3:n.1676_1678delinsAGC
XR_934514.1:n.1248_1250delinsAGC
XR_934514.3:n.1679_1681delinsAGC
XR_934886.1:n.149+3951_149+3953delinsGCT
XR_934886.2:n.149+3951_149+3953delinsGCT