Canonical Allele Identifier: CA3261180624
Community Standard Title: NM_058216.3(RAD51C):c.1097_1098delinsAA (p.Arg366Gln)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734188_58734189delinsAA , CM000679.2:g.58734188_58734189delinsAA GRCh38
NC_000017.10:g.56811549_56811550delinsAA , CM000679.1:g.56811549_56811550delinsAA GRCh37
NC_000017.9:g.54166548_54166549delinsAA NCBI36
NG_023199.1:g.46587_46588delinsAA , LRG_314:g.46587_46588delinsAA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1097_1098delinsAA MANE Select NP_478123.1:p.Arg366Gln
ENST00000337432.9:c.1097_1098delinsAA MANE Select ENSP00000336701.4:p.Arg366Gln
NM_058216.2:c.1097_1098delinsAA NP_478123.1:p.Arg366Gln
NR_103872.1:n.1001_1002delinsAA
NR_103872.2:n.972_973delinsAA
ENST00000337432.8:c.1097_1098delinsAA ENSP00000336701.4:p.Arg366Gln
ENST00000413590.5:c.738_739delinsAA
ENST00000461271.6:c.*1629_*1630delinsAA ENSP00000464056.2:n.*1629_*1630delinsAA
ENST00000461706.1:n.284_285delinsAA
ENST00000475762.5:c.*1733_*1734delinsAA ENSP00000432421.1:n.*1733_*1734delinsAA
ENST00000482007.5:c.*525_*526delinsAA ENSP00000433332.1:n.*525_*526delinsAA
ENST00000487525.5:c.*673_*674delinsAA ENSP00000431637.1:n.*673_*674delinsAA
ENST00000578151.1:n.310_311delinsAA
ENST00000581221.5:n.612_613delinsAA
ENST00000584804.1:c.331_332delinsAA ENSP00000463658.1:n.331_332delinsAA
ENST00000697680.1:c.*2061_*2062delinsAA ENSP00000513392.1:n.*2061_*2062delinsAA
ENST00000697681.1:c.*2258_*2259delinsAA ENSP00000513393.1:n.*2258_*2259delinsAA
ENST00000697683.1:c.*2033_*2034delinsAA ENSP00000513395.1:n.*2033_*2034delinsAA
ENST00000697685.1:c.*1794_*1795delinsAA ENSP00000513396.1:n.*1794_*1795delinsAA
ENST00000697686.1:c.*7_*8delinsAA ENSP00000513397.1:n.*7_*8delinsAA
ENST00000697689.1:c.*1511_*1512delinsAA ENSP00000513398.1:n.*1511_*1512delinsAA
ENST00000697690.1:c.*57_*58delinsAA ENSP00000513399.1:n.*57_*58delinsAA
ENST00000697691.1:c.*1069_*1070delinsAA ENSP00000513400.1:n.*1069_*1070delinsAA
ENST00000697692.1:c.*1109_*1110delinsAA ENSP00000513401.1:n.*1109_*1110delinsAA
ENST00000697694.1:c.746_747delinsAA ENSP00000513402.1:p.Arg249Gln
ENST00000697695.1:n.1704_1705delinsAA
XM_006722001.2:c.1100_1101delinsAA XP_006722064.1:p.Arg367Gln
XM_006722001.4:c.1100_1101delinsAA XP_006722064.1:p.Arg367Gln
XM_006722002.2:c.*7_*8delinsAA XP_006722065.1:n.*7_*8delinsAA
XM_006722002.4:c.*7_*8delinsAA XP_006722065.1:n.*7_*8delinsAA
XM_006722004.2:c.749_750delinsAA XP_006722067.1:p.Arg250Gln
XM_006722004.3:c.749_750delinsAA XP_006722067.1:p.Arg250Gln
XM_006722005.2:c.749_750delinsAA XP_006722068.1:p.Arg250Gln
XM_006722005.3:c.749_750delinsAA XP_006722068.1:p.Arg250Gln
XM_011525092.1:c.749_750delinsAA XP_011523394.1:p.Arg250Gln
XM_011525092.2:c.749_750delinsAA XP_011523394.1:p.Arg250Gln
XM_011525093.1:c.749_750delinsAA XP_011523395.1:p.Arg250Gln
XM_011525093.2:c.749_750delinsAA XP_011523395.1:p.Arg250Gln
XM_011525094.1:c.749_750delinsAA XP_011523396.1:p.Arg250Gln
XM_011525094.2:c.749_750delinsAA XP_011523396.1:p.Arg250Gln
XM_017024914.1:c.746_747delinsAA XP_016880403.1:p.Arg249Gln
XM_017024915.1:c.746_747delinsAA XP_016880404.1:p.Arg249Gln
XM_017024916.1:c.746_747delinsAA XP_016880405.1:p.Arg249Gln
XM_017024917.1:c.746_747delinsAA XP_016880406.1:p.Arg249Gln
XM_017024918.2:c.746_747delinsAA XP_016880407.1:p.Arg249Gln
XM_017024919.1:c.*7_*8delinsAA XP_016880408.1:n.*7_*8delinsAA
XR_934513.1:n.1315_1316delinsAA
XR_934513.3:n.1746_1747delinsAA
XR_934886.1:n.149+3882_149+3883delinsTT
XR_934886.2:n.149+3882_149+3883delinsTT