Canonical Allele Identifier: CA3261179801
Community Standard Title: NM_058216.3(RAD51C):c.779_780delinsAA (p.Arg260Gln)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709932_58709933delinsAA , CM000679.2:g.58709932_58709933delinsAA GRCh38
NC_000017.10:g.56787293_56787294delinsAA , CM000679.1:g.56787293_56787294delinsAA GRCh37
NC_000017.9:g.54142292_54142293delinsAA NCBI36
NG_023199.1:g.22331_22332delinsAA , LRG_314:g.22331_22332delinsAA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.779_780delinsAA MANE Select NP_478123.1:p.Arg260Gln
ENST00000337432.9:c.779_780delinsAA MANE Select ENSP00000336701.4:p.Arg260Gln
NM_058216.2:c.779_780delinsAA NP_478123.1:p.Arg260Gln
NR_103872.1:n.683_684delinsAA
NR_103872.2:n.654_655delinsAA
ENST00000337432.8:c.779_780delinsAA ENSP00000336701.4:p.Arg260Gln
ENST00000413590.5:c.417_418delinsAA
ENST00000461271.6:c.428_429delinsAA ENSP00000464056.2:p.Arg143Gln
ENST00000475762.5:c.*1482_*1483delinsAA ENSP00000432421.1:n.*1482_*1483delinsAA
ENST00000482007.5:c.*207_*208delinsAA ENSP00000433332.1:n.*207_*208delinsAA
ENST00000487525.5:c.*352_*353delinsAA ENSP00000431637.1:n.*352_*353delinsAA
ENST00000578151.1:n.114_115delinsAA
ENST00000581221.5:n.294_295delinsAA
ENST00000583539.5:c.779_780delinsAA ENSP00000463121.1:p.Arg260Gln
ENST00000584617.5:c.501_502delinsAA
ENST00000584804.1:c.74_75delinsAA ENSP00000463658.1:p.Arg25Gln
ENST00000697678.1:n.681_682delinsAA
ENST00000697679.1:n.1853_1854delinsAA
ENST00000697680.1:c.*1643_*1644delinsAA ENSP00000513392.1:n.*1643_*1644delinsAA
ENST00000697681.1:c.*1940_*1941delinsAA ENSP00000513393.1:n.*1940_*1941delinsAA
ENST00000697683.1:c.*1643_*1644delinsAA ENSP00000513395.1:n.*1643_*1644delinsAA
ENST00000697684.1:n.839_840delinsAA
ENST00000697685.1:c.*1476_*1477delinsAA ENSP00000513396.1:n.*1476_*1477delinsAA
ENST00000697686.1:c.428_429delinsAA ENSP00000513397.1:p.Arg143Gln
ENST00000697687.1:n.658_659delinsAA
ENST00000697688.1:n.825_826delinsAA
ENST00000697689.1:c.*1315_*1316delinsAA ENSP00000513398.1:n.*1315_*1316delinsAA
ENST00000697690.1:c.779_780delinsAA ENSP00000513399.1:p.Arg260Gln
ENST00000697691.1:c.*751_*752delinsAA ENSP00000513400.1:n.*751_*752delinsAA
ENST00000697692.1:c.*791_*792delinsAA ENSP00000513401.1:n.*791_*792delinsAA
ENST00000697694.1:c.428_429delinsAA ENSP00000513402.1:p.Arg143Gln
ENST00000697695.1:n.1386_1387delinsAA
XM_006722001.2:c.779_780delinsAA XP_006722064.1:p.Arg260Gln
XM_006722001.4:c.779_780delinsAA XP_006722064.1:p.Arg260Gln
XM_006722002.2:c.779_780delinsAA XP_006722065.1:p.Arg260Gln
XM_006722002.4:c.779_780delinsAA XP_006722065.1:p.Arg260Gln
XM_006722004.2:c.428_429delinsAA XP_006722067.1:p.Arg143Gln
XM_006722004.3:c.428_429delinsAA XP_006722067.1:p.Arg143Gln
XM_006722005.2:c.428_429delinsAA XP_006722068.1:p.Arg143Gln
XM_006722005.3:c.428_429delinsAA XP_006722068.1:p.Arg143Gln
XM_011525092.1:c.428_429delinsAA XP_011523394.1:p.Arg143Gln
XM_011525092.2:c.428_429delinsAA XP_011523394.1:p.Arg143Gln
XM_011525093.1:c.428_429delinsAA XP_011523395.1:p.Arg143Gln
XM_011525093.2:c.428_429delinsAA XP_011523395.1:p.Arg143Gln
XM_011525094.1:c.428_429delinsAA XP_011523396.1:p.Arg143Gln
XM_011525094.2:c.428_429delinsAA XP_011523396.1:p.Arg143Gln
XM_017024914.1:c.428_429delinsAA XP_016880403.1:p.Arg143Gln
XM_017024915.1:c.428_429delinsAA XP_016880404.1:p.Arg143Gln
XM_017024916.1:c.428_429delinsAA XP_016880405.1:p.Arg143Gln
XM_017024917.1:c.428_429delinsAA XP_016880406.1:p.Arg143Gln
XM_017024918.2:c.428_429delinsAA XP_016880407.1:p.Arg143Gln
XM_017024919.1:c.428_429delinsAA XP_016880408.1:p.Arg143Gln
XR_934513.1:n.997_998delinsAA
XR_934513.3:n.1428_1429delinsAA
XR_934514.1:n.997_998delinsAA
XR_934514.3:n.1428_1429delinsAA