Canonical Allele Identifier: CA3261179808
Community Standard Title: NM_058216.3(RAD51C):c.932_933delinsCC (p.Ile311Thr)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724067_58724068delinsCC , CM000679.2:g.58724067_58724068delinsCC GRCh38
NC_000017.10:g.56801428_56801429delinsCC , CM000679.1:g.56801428_56801429delinsCC GRCh37
NC_000017.9:g.54156427_54156428delinsCC NCBI36
NG_023199.1:g.36466_36467delinsCC , LRG_314:g.36466_36467delinsCC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.932_933delinsCC MANE Select NP_478123.1:p.Ile311Thr
ENST00000337432.9:c.932_933delinsCC MANE Select ENSP00000336701.4:p.Ile311Thr
NM_058216.2:c.932_933delinsCC NP_478123.1:p.Ile311Thr
NR_103872.1:n.836_837delinsCC
NR_103872.2:n.807_808delinsCC
ENST00000337432.8:c.932_933delinsCC ENSP00000336701.4:p.Ile311Thr
ENST00000413590.5:c.570_571delinsCC
ENST00000461271.6:c.581_582delinsCC ENSP00000464056.2:p.Ile194Thr
ENST00000475762.5:c.*1568_*1569delinsCC ENSP00000432421.1:n.*1568_*1569delinsCC
ENST00000482007.5:c.*360_*361delinsCC ENSP00000433332.1:n.*360_*361delinsCC
ENST00000487525.5:c.*505_*506delinsCC ENSP00000431637.1:n.*505_*506delinsCC
ENST00000578151.1:n.239+3255_239+3256delinsCC
ENST00000581221.5:n.447_448delinsCC
ENST00000583539.5:c.932_933delinsCC ENSP00000463121.1:p.Ile311Thr
ENST00000584617.5:c.654_655delinsCC
ENST00000584804.1:c.199+3255_199+3256delinsCC ENSP00000463658.1:n.199+3255_199+3256delinsCC
ENST00000697680.1:c.*1896_*1897delinsCC ENSP00000513392.1:n.*1896_*1897delinsCC
ENST00000697681.1:c.*2093_*2094delinsCC ENSP00000513393.1:n.*2093_*2094delinsCC
ENST00000697683.1:c.*1796_*1797delinsCC ENSP00000513395.1:n.*1796_*1797delinsCC
ENST00000697684.1:n.992_993delinsCC
ENST00000697685.1:c.*1629_*1630delinsCC ENSP00000513396.1:n.*1629_*1630delinsCC
ENST00000697686.1:c.581_582delinsCC ENSP00000513397.1:p.Ile194Thr
ENST00000697687.1:n.811_812delinsCC
ENST00000697688.1:n.978_979delinsCC
ENST00000697689.1:c.*1440+3255_*1440+3256delinsCC ENSP00000513398.1:n.*1440+3255_*1440+3256delinsCC
ENST00000697690.1:c.904+3255_904+3256delinsCC ENSP00000513399.1:n.904+3255_904+3256delinsCC
ENST00000697691.1:c.*904_*905delinsCC ENSP00000513400.1:n.*904_*905delinsCC
ENST00000697692.1:c.*944_*945delinsCC ENSP00000513401.1:n.*944_*945delinsCC
ENST00000697694.1:c.581_582delinsCC ENSP00000513402.1:p.Ile194Thr
ENST00000697695.1:n.1539_1540delinsCC
XM_006722001.2:c.932_933delinsCC XP_006722064.1:p.Ile311Thr
XM_006722001.4:c.932_933delinsCC XP_006722064.1:p.Ile311Thr
XM_006722002.2:c.904+3255_904+3256delinsCC XP_006722065.1:n.904+3255_904+3256delinsCC
XM_006722002.4:c.904+3255_904+3256delinsCC XP_006722065.1:n.904+3255_904+3256delinsCC
XM_006722004.2:c.581_582delinsCC XP_006722067.1:p.Ile194Thr
XM_006722004.3:c.581_582delinsCC XP_006722067.1:p.Ile194Thr
XM_006722005.2:c.581_582delinsCC XP_006722068.1:p.Ile194Thr
XM_006722005.3:c.581_582delinsCC XP_006722068.1:p.Ile194Thr
XM_011525092.1:c.581_582delinsCC XP_011523394.1:p.Ile194Thr
XM_011525092.2:c.581_582delinsCC XP_011523394.1:p.Ile194Thr
XM_011525093.1:c.581_582delinsCC XP_011523395.1:p.Ile194Thr
XM_011525093.2:c.581_582delinsCC XP_011523395.1:p.Ile194Thr
XM_011525094.1:c.581_582delinsCC XP_011523396.1:p.Ile194Thr
XM_011525094.2:c.581_582delinsCC XP_011523396.1:p.Ile194Thr
XM_017024914.1:c.581_582delinsCC XP_016880403.1:p.Ile194Thr
XM_017024915.1:c.581_582delinsCC XP_016880404.1:p.Ile194Thr
XM_017024916.1:c.581_582delinsCC XP_016880405.1:p.Ile194Thr
XM_017024917.1:c.581_582delinsCC XP_016880406.1:p.Ile194Thr
XM_017024918.2:c.581_582delinsCC XP_016880407.1:p.Ile194Thr
XM_017024919.1:c.553+3255_553+3256delinsCC XP_016880408.1:n.553+3255_553+3256delinsCC
XR_934513.1:n.1150_1151delinsCC
XR_934513.3:n.1581_1582delinsCC
XR_934514.1:n.1150_1151delinsCC
XR_934514.3:n.1581_1582delinsCC