Canonical Allele Identifier: CA3261180354
Community Standard Title: NM_058216.3(RAD51C):c.1073_1074delinsGG (p.Gln358Arg)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734164_58734165delinsGG , CM000679.2:g.58734164_58734165delinsGG GRCh38
NC_000017.10:g.56811525_56811526delinsGG , CM000679.1:g.56811525_56811526delinsGG GRCh37
NC_000017.9:g.54166524_54166525delinsGG NCBI36
NG_023199.1:g.46563_46564delinsGG , LRG_314:g.46563_46564delinsGG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1073_1074delinsGG MANE Select NP_478123.1:p.Gln358Arg
ENST00000337432.9:c.1073_1074delinsGG MANE Select ENSP00000336701.4:p.Gln358Arg
NM_058216.2:c.1073_1074delinsGG NP_478123.1:p.Gln358Arg
NR_103872.1:n.977_978delinsGG
NR_103872.2:n.948_949delinsGG
ENST00000337432.8:c.1073_1074delinsGG ENSP00000336701.4:p.Gln358Arg
ENST00000413590.5:c.714_715delinsGG
ENST00000461271.6:c.*1605_*1606delinsGG ENSP00000464056.2:n.*1605_*1606delinsGG
ENST00000461706.1:n.260_261delinsGG
ENST00000475762.5:c.*1709_*1710delinsGG ENSP00000432421.1:n.*1709_*1710delinsGG
ENST00000482007.5:c.*501_*502delinsGG ENSP00000433332.1:n.*501_*502delinsGG
ENST00000487525.5:c.*649_*650delinsGG ENSP00000431637.1:n.*649_*650delinsGG
ENST00000578151.1:n.286_287delinsGG
ENST00000581221.5:n.588_589delinsGG
ENST00000584804.1:c.307_308delinsGG ENSP00000463658.1:p.Lys103Gly
ENST00000697680.1:c.*2037_*2038delinsGG ENSP00000513392.1:n.*2037_*2038delinsGG
ENST00000697681.1:c.*2234_*2235delinsGG ENSP00000513393.1:n.*2234_*2235delinsGG
ENST00000697683.1:c.*2009_*2010delinsGG ENSP00000513395.1:n.*2009_*2010delinsGG
ENST00000697685.1:c.*1770_*1771delinsGG ENSP00000513396.1:n.*1770_*1771delinsGG
ENST00000697686.1:c.844_845delinsGG ENSP00000513397.1:p.Lys282Gly
ENST00000697689.1:c.*1487_*1488delinsGG ENSP00000513398.1:n.*1487_*1488delinsGG
ENST00000697690.1:c.*33_*34delinsGG ENSP00000513399.1:n.*33_*34delinsGG
ENST00000697691.1:c.*1045_*1046delinsGG ENSP00000513400.1:n.*1045_*1046delinsGG
ENST00000697692.1:c.*1085_*1086delinsGG ENSP00000513401.1:n.*1085_*1086delinsGG
ENST00000697694.1:c.722_723delinsGG ENSP00000513402.1:p.Gln241Arg
ENST00000697695.1:n.1680_1681delinsGG
XM_006722001.2:c.1076_1077delinsGG XP_006722064.1:p.Gln359Arg
XM_006722001.4:c.1076_1077delinsGG XP_006722064.1:p.Gln359Arg
XM_006722002.2:c.1012_1013delinsGG XP_006722065.1:p.Lys338Gly
XM_006722002.4:c.1012_1013delinsGG XP_006722065.1:p.Lys338Gly
XM_006722004.2:c.725_726delinsGG XP_006722067.1:p.Gln242Arg
XM_006722004.3:c.725_726delinsGG XP_006722067.1:p.Gln242Arg
XM_006722005.2:c.725_726delinsGG XP_006722068.1:p.Gln242Arg
XM_006722005.3:c.725_726delinsGG XP_006722068.1:p.Gln242Arg
XM_011525092.1:c.725_726delinsGG XP_011523394.1:p.Gln242Arg
XM_011525092.2:c.725_726delinsGG XP_011523394.1:p.Gln242Arg
XM_011525093.1:c.725_726delinsGG XP_011523395.1:p.Gln242Arg
XM_011525093.2:c.725_726delinsGG XP_011523395.1:p.Gln242Arg
XM_011525094.1:c.725_726delinsGG XP_011523396.1:p.Gln242Arg
XM_011525094.2:c.725_726delinsGG XP_011523396.1:p.Gln242Arg
XM_017024914.1:c.722_723delinsGG XP_016880403.1:p.Gln241Arg
XM_017024915.1:c.722_723delinsGG XP_016880404.1:p.Gln241Arg
XM_017024916.1:c.722_723delinsGG XP_016880405.1:p.Gln241Arg
XM_017024917.1:c.722_723delinsGG XP_016880406.1:p.Gln241Arg
XM_017024918.2:c.722_723delinsGG XP_016880407.1:p.Gln241Arg
XM_017024919.1:c.661_662delinsGG XP_016880408.1:p.Lys221Gly
XR_934513.1:n.1291_1292delinsGG
XR_934513.3:n.1722_1723delinsGG
XR_934514.1:n.1294_1295delinsGG
XR_934514.3:n.1725_1726delinsGG
XR_934886.1:n.149+3906_149+3907delinsCC
XR_934886.2:n.149+3906_149+3907delinsCC