Canonical Allele Identifier: CA3057228132

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692662_58692663delinsTC , CM000679.2:g.58692662_58692663delinsTC	GRCh38
NC_000017.10:g.56770023_56770024delinsTC , CM000679.1:g.56770023_56770024delinsTC	GRCh37
NC_000017.9:g.54125022_54125023delinsTC	NCBI36
NG_023199.1:g.5061_5062delinsTC , LRG_314:g.5061_5062delinsTC
NG_047169.1:g.4417_4418delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-230_-229delinsTC	ENSP00000464056.2:n.-230_-229delinsTC
ENST00000697675.1:n.90_91delinsTC
ENST00000697676.1:n.79_80delinsTC
ENST00000697677.1:n.77_78delinsTC
ENST00000697678.1:n.47+30_47+31delinsTC
ENST00000697679.1:n.70_71delinsTC
ENST00000697680.1:c.19_20delinsTC	ENSP00000513392.1:p.Arg7Ser
ENST00000697681.1:c.19_20delinsTC	ENSP00000513393.1:p.Arg7Ser
ENST00000697683.1:c.19_20delinsTC	ENSP00000513395.1:p.Arg7Ser
ENST00000697684.1:n.79_80delinsTC
ENST00000697685.1:c.19_20delinsTC	ENSP00000513396.1:p.Arg7Ser
ENST00000697686.1:c.-207+30_-207+31delinsTC	ENSP00000513397.1:n.-207+30_-207+31delinsTC
ENST00000697687.1:n.65_66delinsTC
ENST00000697688.1:n.65_66delinsTC
ENST00000697689.1:c.19_20delinsTC	ENSP00000513398.1:p.Arg7Ser
ENST00000697690.1:c.19_20delinsTC	ENSP00000513399.1:p.Arg7Ser
ENST00000697691.1:c.19_20delinsTC	ENSP00000513400.1:p.Arg7Ser
ENST00000697692.1:c.19_20delinsTC	ENSP00000513401.1:p.Arg7Ser
ENST00000337432.9:c.19_20delinsTC MANE Select	ENSP00000336701.4:p.Arg7Ser
ENST00000337432.8:c.19_20delinsTC	ENSP00000336701.4:p.Arg7Ser
ENST00000421782.3:c.19_20delinsTC	ENSP00000391450.2:p.Arg7Ser
ENST00000461271.5:c.-230_-229delinsTC	ENSP00000464056.1:n.-230_-229delinsTC
ENST00000475762.5:c.19_20delinsTC	ENSP00000432421.1:p.Arg7Ser
ENST00000476741.2:n.61_62delinsTC
ENST00000482007.5:c.19_20delinsTC	ENSP00000433332.1:p.Arg7Ser
ENST00000486827.1:c.19_20delinsTC	ENSP00000436761.1:p.Arg7Ser
ENST00000487525.5:c.19_20delinsTC	ENSP00000431637.1:p.Arg7Ser
ENST00000487921.5:n.57+30_57+31delinsTC
ENST00000583539.5:c.19_20delinsTC	ENSP00000463121.1:p.Arg7Ser
NM_002876.3:c.19_20delinsTC	NP_002867.1:p.Arg7Ser
NM_058216.2:c.19_20delinsTC	NP_478123.1:p.Arg7Ser
NR_103872.1:n.90_91delinsTC
NR_103873.1:n.90_91delinsTC
XM_006722001.2:c.19_20delinsTC	XP_006722064.1:p.Arg7Ser
XM_006722002.2:c.19_20delinsTC	XP_006722065.1:p.Arg7Ser
XM_006722004.2:c.-230_-229delinsTC	XP_006722067.1:n.-230_-229delinsTC
XM_006722005.2:c.-207+30_-207+31delinsTC	XP_006722068.1:n.-207+30_-207+31delinsTC
XM_011525092.1:c.-530_-529delinsTC	XP_011523394.1:n.-530_-529delinsTC
XM_011525093.1:c.-691_-690delinsTC	XP_011523395.1:n.-691_-690delinsTC
XR_934513.1:n.92_93delinsTC
XR_934514.1:n.92_93delinsTC
XM_006722001.4:c.19_20delinsTC	XP_006722064.1:p.Arg7Ser
XM_006722002.4:c.19_20delinsTC	XP_006722065.1:p.Arg7Ser
XM_006722004.3:c.-230_-229delinsTC	XP_006722067.1:n.-230_-229delinsTC
XM_006722005.3:c.-207+30_-207+31delinsTC	XP_006722068.1:n.-207+30_-207+31delinsTC
XM_017024914.1:c.-230_-229delinsTC	XP_016880403.1:n.-230_-229delinsTC
XM_017024916.1:c.-530_-529delinsTC	XP_016880405.1:n.-530_-529delinsTC
XM_017024917.1:c.-207+30_-207+31delinsTC	XP_016880406.1:n.-207+30_-207+31delinsTC
XM_017024918.2:c.-504_-503delinsTC	XP_016880407.1:n.-504_-503delinsTC
XR_934513.3:n.523_524delinsTC
XR_934514.3:n.523_524delinsTC
NM_058216.3:c.19_20delinsTC MANE Select	NP_478123.1:p.Arg7Ser
NR_103872.2:n.61_62delinsTC
NM_002876.4:c.19_20delinsTC	NP_002867.1:p.Arg7Ser