Canonical Allele Identifier: CA3261179089
Community Standard Title: NM_058216.3(RAD51C):c.605_606delinsGC (p.Asp202Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58703229_58703230delinsGC , CM000679.2:g.58703229_58703230delinsGC GRCh38
NC_000017.10:g.56780590_56780591delinsGC , CM000679.1:g.56780590_56780591delinsGC GRCh37
NC_000017.9:g.54135589_54135590delinsGC NCBI36
NG_023199.1:g.15628_15629delinsGC , LRG_314:g.15628_15629delinsGC

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.605_606delinsGC MANE Select NP_478123.1:p.Asp202Gly
ENST00000337432.9:c.605_606delinsGC MANE Select ENSP00000336701.4:p.Asp202Gly
NM_058216.2:c.605_606delinsGC NP_478123.1:p.Asp202Gly
NR_103872.1:n.509_510delinsGC
NR_103872.2:n.480_481delinsGC
ENST00000337432.8:c.605_606delinsGC ENSP00000336701.4:p.Asp202Gly
ENST00000413590.5:c.243_244delinsGC
ENST00000425173.5:c.401_402delinsGC ENSP00000407282.1:p.Asp134Gly
ENST00000461271.5:c.254_255delinsGC ENSP00000464056.1:p.Asp85Gly
ENST00000461271.6:c.254_255delinsGC ENSP00000464056.2:p.Asp85Gly
ENST00000475762.5:c.*1308_*1309delinsGC ENSP00000432421.1:n.*1308_*1309delinsGC
ENST00000482007.5:c.*33_*34delinsGC ENSP00000433332.1:n.*33_*34delinsGC
ENST00000487525.5:c.*33_*34delinsGC ENSP00000431637.1:n.*33_*34delinsGC
ENST00000487921.5:n.517_518delinsGC
ENST00000583539.5:c.605_606delinsGC ENSP00000463121.1:p.Asp202Gly
ENST00000584617.5:c.327_328delinsGC
ENST00000697677.1:n.1686_1687delinsGC
ENST00000697678.1:n.507_508delinsGC
ENST00000697679.1:n.1679_1680delinsGC
ENST00000697680.1:c.*1469_*1470delinsGC ENSP00000513392.1:n.*1469_*1470delinsGC
ENST00000697681.1:c.*1621_*1622delinsGC ENSP00000513393.1:n.*1621_*1622delinsGC
ENST00000697683.1:c.*1469_*1470delinsGC ENSP00000513395.1:n.*1469_*1470delinsGC
ENST00000697684.1:n.665_666delinsGC
ENST00000697685.1:c.*1302_*1303delinsGC ENSP00000513396.1:n.*1302_*1303delinsGC
ENST00000697686.1:c.254_255delinsGC ENSP00000513397.1:p.Asp85Gly
ENST00000697687.1:n.484_485delinsGC
ENST00000697688.1:n.651_652delinsGC
ENST00000697689.1:c.*1141_*1142delinsGC ENSP00000513398.1:n.*1141_*1142delinsGC
ENST00000697690.1:c.605_606delinsGC ENSP00000513399.1:p.Asp202Gly
ENST00000697691.1:c.*577_*578delinsGC ENSP00000513400.1:n.*577_*578delinsGC
ENST00000697692.1:c.*617_*618delinsGC ENSP00000513401.1:n.*617_*618delinsGC
ENST00000697694.1:c.254_255delinsGC ENSP00000513402.1:p.Asp85Gly
ENST00000697695.1:n.1212_1213delinsGC
XM_006722001.2:c.605_606delinsGC XP_006722064.1:p.Asp202Gly
XM_006722001.4:c.605_606delinsGC XP_006722064.1:p.Asp202Gly
XM_006722002.2:c.605_606delinsGC XP_006722065.1:p.Asp202Gly
XM_006722002.4:c.605_606delinsGC XP_006722065.1:p.Asp202Gly
XM_006722004.2:c.254_255delinsGC XP_006722067.1:p.Asp85Gly
XM_006722004.3:c.254_255delinsGC XP_006722067.1:p.Asp85Gly
XM_006722005.2:c.254_255delinsGC XP_006722068.1:p.Asp85Gly
XM_006722005.3:c.254_255delinsGC XP_006722068.1:p.Asp85Gly
XM_011525092.1:c.254_255delinsGC XP_011523394.1:p.Asp85Gly
XM_011525092.2:c.254_255delinsGC XP_011523394.1:p.Asp85Gly
XM_011525093.1:c.254_255delinsGC XP_011523395.1:p.Asp85Gly
XM_011525093.2:c.254_255delinsGC XP_011523395.1:p.Asp85Gly
XM_011525094.1:c.254_255delinsGC XP_011523396.1:p.Asp85Gly
XM_011525094.2:c.254_255delinsGC XP_011523396.1:p.Asp85Gly
XM_017024914.1:c.254_255delinsGC XP_016880403.1:p.Asp85Gly
XM_017024915.1:c.254_255delinsGC XP_016880404.1:p.Asp85Gly
XM_017024916.1:c.254_255delinsGC XP_016880405.1:p.Asp85Gly
XM_017024917.1:c.254_255delinsGC XP_016880406.1:p.Asp85Gly
XM_017024918.2:c.254_255delinsGC XP_016880407.1:p.Asp85Gly
XM_017024919.1:c.254_255delinsGC XP_016880408.1:p.Asp85Gly
XR_934513.1:n.678_679delinsGC
XR_934513.3:n.1109_1110delinsGC
XR_934514.1:n.678_679delinsGC
XR_934514.3:n.1109_1110delinsGC