Canonical Allele Identifier: CA3261179681
Community Standard Title: NM_058216.3(RAD51C):c.923_924delinsGC (p.Ala308Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724058_58724059delinsGC , CM000679.2:g.58724058_58724059delinsGC GRCh38
NC_000017.10:g.56801419_56801420delinsGC , CM000679.1:g.56801419_56801420delinsGC GRCh37
NC_000017.9:g.54156418_54156419delinsGC NCBI36
NG_023199.1:g.36457_36458delinsGC , LRG_314:g.36457_36458delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.923_924delinsGC MANE Select NP_478123.1:p.Ala308Gly
ENST00000337432.9:c.923_924delinsGC MANE Select ENSP00000336701.4:p.Ala308Gly
NM_058216.2:c.923_924delinsGC NP_478123.1:p.Ala308Gly
NR_103872.1:n.827_828delinsGC
NR_103872.2:n.798_799delinsGC
ENST00000337432.8:c.923_924delinsGC ENSP00000336701.4:p.Ala308Gly
ENST00000413590.5:c.561_562delinsGC
ENST00000461271.6:c.572_573delinsGC ENSP00000464056.2:p.Ala191Gly
ENST00000475762.5:c.*1559_*1560delinsGC ENSP00000432421.1:n.*1559_*1560delinsGC
ENST00000482007.5:c.*351_*352delinsGC ENSP00000433332.1:n.*351_*352delinsGC
ENST00000487525.5:c.*496_*497delinsGC ENSP00000431637.1:n.*496_*497delinsGC
ENST00000578151.1:n.239+3246_239+3247delinsGC
ENST00000581221.5:n.438_439delinsGC
ENST00000583539.5:c.923_924delinsGC ENSP00000463121.1:p.Ala308Gly
ENST00000584617.5:c.645_646delinsGC
ENST00000584804.1:c.199+3246_199+3247delinsGC ENSP00000463658.1:n.199+3246_199+3247delinsGC
ENST00000697680.1:c.*1887_*1888delinsGC ENSP00000513392.1:n.*1887_*1888delinsGC
ENST00000697681.1:c.*2084_*2085delinsGC ENSP00000513393.1:n.*2084_*2085delinsGC
ENST00000697683.1:c.*1787_*1788delinsGC ENSP00000513395.1:n.*1787_*1788delinsGC
ENST00000697684.1:n.983_984delinsGC
ENST00000697685.1:c.*1620_*1621delinsGC ENSP00000513396.1:n.*1620_*1621delinsGC
ENST00000697686.1:c.572_573delinsGC ENSP00000513397.1:p.Ala191Gly
ENST00000697687.1:n.802_803delinsGC
ENST00000697688.1:n.969_970delinsGC
ENST00000697689.1:c.*1440+3246_*1440+3247delinsGC ENSP00000513398.1:n.*1440+3246_*1440+3247delinsGC
ENST00000697690.1:c.904+3246_904+3247delinsGC ENSP00000513399.1:n.904+3246_904+3247delinsGC
ENST00000697691.1:c.*895_*896delinsGC ENSP00000513400.1:n.*895_*896delinsGC
ENST00000697692.1:c.*935_*936delinsGC ENSP00000513401.1:n.*935_*936delinsGC
ENST00000697694.1:c.572_573delinsGC ENSP00000513402.1:p.Ala191Gly
ENST00000697695.1:n.1530_1531delinsGC
XM_006722001.2:c.923_924delinsGC XP_006722064.1:p.Ala308Gly
XM_006722001.4:c.923_924delinsGC XP_006722064.1:p.Ala308Gly
XM_006722002.2:c.904+3246_904+3247delinsGC XP_006722065.1:n.904+3246_904+3247delinsGC
XM_006722002.4:c.904+3246_904+3247delinsGC XP_006722065.1:n.904+3246_904+3247delinsGC
XM_006722004.2:c.572_573delinsGC XP_006722067.1:p.Ala191Gly
XM_006722004.3:c.572_573delinsGC XP_006722067.1:p.Ala191Gly
XM_006722005.2:c.572_573delinsGC XP_006722068.1:p.Ala191Gly
XM_006722005.3:c.572_573delinsGC XP_006722068.1:p.Ala191Gly
XM_011525092.1:c.572_573delinsGC XP_011523394.1:p.Ala191Gly
XM_011525092.2:c.572_573delinsGC XP_011523394.1:p.Ala191Gly
XM_011525093.1:c.572_573delinsGC XP_011523395.1:p.Ala191Gly
XM_011525093.2:c.572_573delinsGC XP_011523395.1:p.Ala191Gly
XM_011525094.1:c.572_573delinsGC XP_011523396.1:p.Ala191Gly
XM_011525094.2:c.572_573delinsGC XP_011523396.1:p.Ala191Gly
XM_017024914.1:c.572_573delinsGC XP_016880403.1:p.Ala191Gly
XM_017024915.1:c.572_573delinsGC XP_016880404.1:p.Ala191Gly
XM_017024916.1:c.572_573delinsGC XP_016880405.1:p.Ala191Gly
XM_017024917.1:c.572_573delinsGC XP_016880406.1:p.Ala191Gly
XM_017024918.2:c.572_573delinsGC XP_016880407.1:p.Ala191Gly
XM_017024919.1:c.553+3246_553+3247delinsGC XP_016880408.1:n.553+3246_553+3247delinsGC
XR_934513.1:n.1141_1142delinsGC
XR_934513.3:n.1572_1573delinsGC
XR_934514.1:n.1141_1142delinsGC
XR_934514.3:n.1572_1573delinsGC