Canonical Allele Identifier: CA3057242921

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709942_58709944delinsCTC , CM000679.2:g.58709942_58709944delinsCTC	GRCh38
NC_000017.10:g.56787303_56787305delinsCTC , CM000679.1:g.56787303_56787305delinsCTC	GRCh37
NC_000017.9:g.54142302_54142304delinsCTC	NCBI36
NG_023199.1:g.22341_22343delinsCTC , LRG_314:g.22341_22343delinsCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.438_440delinsCTC	ENSP00000464056.2:p.Gly147Ser
ENST00000697678.1:n.691_693delinsCTC
ENST00000697679.1:n.1863_1865delinsCTC
ENST00000697680.1:c.*1653_*1655delinsCTC	ENSP00000513392.1:n.*1653_*1655delinsCTC
ENST00000697681.1:c.*1950_*1952delinsCTC	ENSP00000513393.1:n.*1950_*1952delinsCTC
ENST00000697683.1:c.*1653_*1655delinsCTC	ENSP00000513395.1:n.*1653_*1655delinsCTC
ENST00000697684.1:n.849_851delinsCTC
ENST00000697685.1:c.*1486_*1488delinsCTC	ENSP00000513396.1:n.*1486_*1488delinsCTC
ENST00000697686.1:c.438_440delinsCTC	ENSP00000513397.1:p.Gly147Ser
ENST00000697687.1:n.668_670delinsCTC
ENST00000697688.1:n.835_837delinsCTC
ENST00000697689.1:c.*1325_*1327delinsCTC	ENSP00000513398.1:n.*1325_*1327delinsCTC
ENST00000697690.1:c.789_791delinsCTC	ENSP00000513399.1:p.Gly264Ser
ENST00000697691.1:c.*761_*763delinsCTC	ENSP00000513400.1:n.*761_*763delinsCTC
ENST00000697692.1:c.*801_*803delinsCTC	ENSP00000513401.1:n.*801_*803delinsCTC
ENST00000697694.1:c.438_440delinsCTC	ENSP00000513402.1:p.Gly147Ser
ENST00000697695.1:n.1396_1398delinsCTC
ENST00000337432.9:c.789_791delinsCTC MANE Select	ENSP00000336701.4:p.Gly264Ser
ENST00000337432.8:c.789_791delinsCTC	ENSP00000336701.4:p.Gly264Ser
ENST00000413590.5:c.427_429delinsCTC
ENST00000475762.5:c.*1492_*1494delinsCTC	ENSP00000432421.1:n.*1492_*1494delinsCTC
ENST00000482007.5:c.*217_*219delinsCTC	ENSP00000433332.1:n.*217_*219delinsCTC
ENST00000487525.5:c.*362_*364delinsCTC	ENSP00000431637.1:n.*362_*364delinsCTC
ENST00000578151.1:n.124_126delinsCTC
ENST00000581221.5:n.304_306delinsCTC
ENST00000583539.5:c.789_791delinsCTC	ENSP00000463121.1:p.Gly264Ser
ENST00000584617.5:c.511_513delinsCTC
ENST00000584804.1:c.84_86delinsCTC	ENSP00000463658.1:p.Gly29Ser
NM_058216.2:c.789_791delinsCTC	NP_478123.1:p.Gly264Ser
NR_103872.1:n.693_695delinsCTC
XM_006722001.2:c.789_791delinsCTC	XP_006722064.1:p.Gly264Ser
XM_006722002.2:c.789_791delinsCTC	XP_006722065.1:p.Gly264Ser
XM_006722004.2:c.438_440delinsCTC	XP_006722067.1:p.Gly147Ser
XM_006722005.2:c.438_440delinsCTC	XP_006722068.1:p.Gly147Ser
XM_011525092.1:c.438_440delinsCTC	XP_011523394.1:p.Gly147Ser
XM_011525093.1:c.438_440delinsCTC	XP_011523395.1:p.Gly147Ser
XM_011525094.1:c.438_440delinsCTC	XP_011523396.1:p.Gly147Ser
XR_934513.1:n.1007_1009delinsCTC
XR_934514.1:n.1007_1009delinsCTC
XM_006722001.4:c.789_791delinsCTC	XP_006722064.1:p.Gly264Ser
XM_006722002.4:c.789_791delinsCTC	XP_006722065.1:p.Gly264Ser
XM_006722004.3:c.438_440delinsCTC	XP_006722067.1:p.Gly147Ser
XM_006722005.3:c.438_440delinsCTC	XP_006722068.1:p.Gly147Ser
XM_011525092.2:c.438_440delinsCTC	XP_011523394.1:p.Gly147Ser
XM_011525093.2:c.438_440delinsCTC	XP_011523395.1:p.Gly147Ser
XM_011525094.2:c.438_440delinsCTC	XP_011523396.1:p.Gly147Ser
XM_017024914.1:c.438_440delinsCTC	XP_016880403.1:p.Gly147Ser
XM_017024915.1:c.438_440delinsCTC	XP_016880404.1:p.Gly147Ser
XM_017024916.1:c.438_440delinsCTC	XP_016880405.1:p.Gly147Ser
XM_017024917.1:c.438_440delinsCTC	XP_016880406.1:p.Gly147Ser
XM_017024918.2:c.438_440delinsCTC	XP_016880407.1:p.Gly147Ser
XM_017024919.1:c.438_440delinsCTC	XP_016880408.1:p.Gly147Ser
XR_934513.3:n.1438_1440delinsCTC
XR_934514.3:n.1438_1440delinsCTC
NM_058216.3:c.789_791delinsCTC MANE Select	NP_478123.1:p.Gly264Ser
NR_103872.2:n.664_666delinsCTC