Canonical Allele Identifier: CA3057228333
Community Standard Title: NM_058216.3(RAD51C):c.834_835delinsGC (p.Ala279Pro)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58709987_58709988delinsGC , CM000679.2:g.58709987_58709988delinsGC GRCh38
NC_000017.10:g.56787348_56787349delinsGC , CM000679.1:g.56787348_56787349delinsGC GRCh37
NC_000017.9:g.54142347_54142348delinsGC NCBI36
NG_023199.1:g.22386_22387delinsGC , LRG_314:g.22386_22387delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.834_835delinsGC MANE Select NP_478123.1:p.Ala279Pro
ENST00000337432.9:c.834_835delinsGC MANE Select ENSP00000336701.4:p.Ala279Pro
NM_058216.2:c.834_835delinsGC NP_478123.1:p.Ala279Pro
NR_103872.1:n.738_739delinsGC
NR_103872.2:n.709_710delinsGC
ENST00000337432.8:c.834_835delinsGC ENSP00000336701.4:p.Ala279Pro
ENST00000413590.5:c.472_473delinsGC
ENST00000461271.6:c.483_484delinsGC ENSP00000464056.2:p.Ala162Pro
ENST00000475762.5:c.*1537_*1538delinsGC ENSP00000432421.1:n.*1537_*1538delinsGC
ENST00000482007.5:c.*262_*263delinsGC ENSP00000433332.1:n.*262_*263delinsGC
ENST00000487525.5:c.*407_*408delinsGC ENSP00000431637.1:n.*407_*408delinsGC
ENST00000578151.1:n.169_170delinsGC
ENST00000581221.5:n.349_350delinsGC
ENST00000583539.5:c.834_835delinsGC ENSP00000463121.1:p.Ala279Pro
ENST00000584617.5:c.556_557delinsGC
ENST00000584804.1:c.129_130delinsGC ENSP00000463658.1:p.Ala44Pro
ENST00000697678.1:n.736_737delinsGC
ENST00000697679.1:n.1908_1909delinsGC
ENST00000697680.1:c.*1698_*1699delinsGC ENSP00000513392.1:n.*1698_*1699delinsGC
ENST00000697681.1:c.*1995_*1996delinsGC ENSP00000513393.1:n.*1995_*1996delinsGC
ENST00000697683.1:c.*1698_*1699delinsGC ENSP00000513395.1:n.*1698_*1699delinsGC
ENST00000697684.1:n.894_895delinsGC
ENST00000697685.1:c.*1531_*1532delinsGC ENSP00000513396.1:n.*1531_*1532delinsGC
ENST00000697686.1:c.483_484delinsGC ENSP00000513397.1:p.Ala162Pro
ENST00000697687.1:n.713_714delinsGC
ENST00000697688.1:n.880_881delinsGC
ENST00000697689.1:c.*1370_*1371delinsGC ENSP00000513398.1:n.*1370_*1371delinsGC
ENST00000697690.1:c.834_835delinsGC ENSP00000513399.1:p.Ala279Pro
ENST00000697691.1:c.*806_*807delinsGC ENSP00000513400.1:n.*806_*807delinsGC
ENST00000697692.1:c.*846_*847delinsGC ENSP00000513401.1:n.*846_*847delinsGC
ENST00000697694.1:c.483_484delinsGC ENSP00000513402.1:p.Ala162Pro
ENST00000697695.1:n.1441_1442delinsGC
XM_006722001.2:c.834_835delinsGC XP_006722064.1:p.Ala279Pro
XM_006722001.4:c.834_835delinsGC XP_006722064.1:p.Ala279Pro
XM_006722002.2:c.834_835delinsGC XP_006722065.1:p.Ala279Pro
XM_006722002.4:c.834_835delinsGC XP_006722065.1:p.Ala279Pro
XM_006722004.2:c.483_484delinsGC XP_006722067.1:p.Ala162Pro
XM_006722004.3:c.483_484delinsGC XP_006722067.1:p.Ala162Pro
XM_006722005.2:c.483_484delinsGC XP_006722068.1:p.Ala162Pro
XM_006722005.3:c.483_484delinsGC XP_006722068.1:p.Ala162Pro
XM_011525092.1:c.483_484delinsGC XP_011523394.1:p.Ala162Pro
XM_011525092.2:c.483_484delinsGC XP_011523394.1:p.Ala162Pro
XM_011525093.1:c.483_484delinsGC XP_011523395.1:p.Ala162Pro
XM_011525093.2:c.483_484delinsGC XP_011523395.1:p.Ala162Pro
XM_011525094.1:c.483_484delinsGC XP_011523396.1:p.Ala162Pro
XM_011525094.2:c.483_484delinsGC XP_011523396.1:p.Ala162Pro
XM_017024914.1:c.483_484delinsGC XP_016880403.1:p.Ala162Pro
XM_017024915.1:c.483_484delinsGC XP_016880404.1:p.Ala162Pro
XM_017024916.1:c.483_484delinsGC XP_016880405.1:p.Ala162Pro
XM_017024917.1:c.483_484delinsGC XP_016880406.1:p.Ala162Pro
XM_017024918.2:c.483_484delinsGC XP_016880407.1:p.Ala162Pro
XM_017024919.1:c.483_484delinsGC XP_016880408.1:p.Ala162Pro
XR_934513.1:n.1052_1053delinsGC
XR_934513.3:n.1483_1484delinsGC
XR_934514.1:n.1052_1053delinsGC
XR_934514.3:n.1483_1484delinsGC