Canonical Allele Identifier: CA3057243490
Community Standard Title: NM_058216.3(RAD51C):c.1030_1031delinsTG (p.Gln344Trp)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734121_58734122delinsTG , CM000679.2:g.58734121_58734122delinsTG GRCh38
NC_000017.10:g.56811482_56811483delinsTG , CM000679.1:g.56811482_56811483delinsTG GRCh37
NC_000017.9:g.54166481_54166482delinsTG NCBI36
NG_023199.1:g.46520_46521delinsTG , LRG_314:g.46520_46521delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1030_1031delinsTG MANE Select NP_478123.1:p.Gln344Trp
ENST00000337432.9:c.1030_1031delinsTG MANE Select ENSP00000336701.4:p.Gln344Trp
NM_058216.2:c.1030_1031delinsTG NP_478123.1:p.Gln344Trp
NR_103872.1:n.934_935delinsTG
NR_103872.2:n.905_906delinsTG
ENST00000337432.8:c.1030_1031delinsTG ENSP00000336701.4:p.Gln344Trp
ENST00000413590.5:c.671_672delinsTG
ENST00000461271.6:c.*1562_*1563delinsTG ENSP00000464056.2:n.*1562_*1563delinsTG
ENST00000461706.1:n.217_218delinsTG
ENST00000475762.5:c.*1666_*1667delinsTG ENSP00000432421.1:n.*1666_*1667delinsTG
ENST00000482007.5:c.*458_*459delinsTG ENSP00000433332.1:n.*458_*459delinsTG
ENST00000487525.5:c.*606_*607delinsTG ENSP00000431637.1:n.*606_*607delinsTG
ENST00000578151.1:n.243_244delinsTG
ENST00000581221.5:n.545_546delinsTG
ENST00000584804.1:c.264_265delinsTG ENSP00000463658.1:p.Arg89Gly
ENST00000697680.1:c.*1994_*1995delinsTG ENSP00000513392.1:n.*1994_*1995delinsTG
ENST00000697681.1:c.*2191_*2192delinsTG ENSP00000513393.1:n.*2191_*2192delinsTG
ENST00000697683.1:c.*1966_*1967delinsTG ENSP00000513395.1:n.*1966_*1967delinsTG
ENST00000697685.1:c.*1727_*1728delinsTG ENSP00000513396.1:n.*1727_*1728delinsTG
ENST00000697686.1:c.801_802delinsTG ENSP00000513397.1:p.Arg268Gly
ENST00000697689.1:c.*1444_*1445delinsTG ENSP00000513398.1:n.*1444_*1445delinsTG
ENST00000697690.1:c.908_909delinsTG ENSP00000513399.1:p.Ser303Leu
ENST00000697691.1:c.*1002_*1003delinsTG ENSP00000513400.1:n.*1002_*1003delinsTG
ENST00000697692.1:c.*1042_*1043delinsTG ENSP00000513401.1:n.*1042_*1043delinsTG
ENST00000697694.1:c.679_680delinsTG ENSP00000513402.1:p.Gln227Trp
ENST00000697695.1:n.1637_1638delinsTG
XM_006722001.2:c.1033_1034delinsTG XP_006722064.1:p.Gln345Trp
XM_006722001.4:c.1033_1034delinsTG XP_006722064.1:p.Gln345Trp
XM_006722002.2:c.969_970delinsTG XP_006722065.1:p.Arg324Gly
XM_006722002.4:c.969_970delinsTG XP_006722065.1:p.Arg324Gly
XM_006722004.2:c.682_683delinsTG XP_006722067.1:p.Gln228Trp
XM_006722004.3:c.682_683delinsTG XP_006722067.1:p.Gln228Trp
XM_006722005.2:c.682_683delinsTG XP_006722068.1:p.Gln228Trp
XM_006722005.3:c.682_683delinsTG XP_006722068.1:p.Gln228Trp
XM_011525092.1:c.682_683delinsTG XP_011523394.1:p.Gln228Trp
XM_011525092.2:c.682_683delinsTG XP_011523394.1:p.Gln228Trp
XM_011525093.1:c.682_683delinsTG XP_011523395.1:p.Gln228Trp
XM_011525093.2:c.682_683delinsTG XP_011523395.1:p.Gln228Trp
XM_011525094.1:c.682_683delinsTG XP_011523396.1:p.Gln228Trp
XM_011525094.2:c.682_683delinsTG XP_011523396.1:p.Gln228Trp
XM_017024914.1:c.679_680delinsTG XP_016880403.1:p.Gln227Trp
XM_017024915.1:c.679_680delinsTG XP_016880404.1:p.Gln227Trp
XM_017024916.1:c.679_680delinsTG XP_016880405.1:p.Gln227Trp
XM_017024917.1:c.679_680delinsTG XP_016880406.1:p.Gln227Trp
XM_017024918.2:c.679_680delinsTG XP_016880407.1:p.Gln227Trp
XM_017024919.1:c.618_619delinsTG XP_016880408.1:p.Arg207Gly
XR_934513.1:n.1248_1249delinsTG
XR_934513.3:n.1679_1680delinsTG
XR_934514.1:n.1251_1252delinsTG
XR_934514.3:n.1682_1683delinsTG
XR_934886.1:n.149+3949_149+3950delinsCA
XR_934886.2:n.149+3949_149+3950delinsCA