Canonical Allele Identifier: CA3057228005

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692659_58692660delinsGA , CM000679.2:g.58692659_58692660delinsGA	GRCh38
NC_000017.10:g.56770020_56770021delinsGA , CM000679.1:g.56770020_56770021delinsGA	GRCh37
NC_000017.9:g.54125019_54125020delinsGA	NCBI36
NG_023199.1:g.5058_5059delinsGA , LRG_314:g.5058_5059delinsGA
NG_047169.1:g.4420_4421delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-233_-232delinsGA	ENSP00000464056.2:n.-233_-232delinsGA
ENST00000697675.1:n.87_88delinsGA
ENST00000697676.1:n.76_77delinsGA
ENST00000697677.1:n.74_75delinsGA
ENST00000697678.1:n.47+27_47+28delinsGA
ENST00000697679.1:n.67_68delinsGA
ENST00000697680.1:c.16_17delinsGA	ENSP00000513392.1:p.Phe6Asp
ENST00000697681.1:c.16_17delinsGA	ENSP00000513393.1:p.Phe6Asp
ENST00000697683.1:c.16_17delinsGA	ENSP00000513395.1:p.Phe6Asp
ENST00000697684.1:n.76_77delinsGA
ENST00000697685.1:c.16_17delinsGA	ENSP00000513396.1:p.Phe6Asp
ENST00000697686.1:c.-207+27_-207+28delinsGA	ENSP00000513397.1:n.-207+27_-207+28delinsGA
ENST00000697687.1:n.62_63delinsGA
ENST00000697688.1:n.62_63delinsGA
ENST00000697689.1:c.16_17delinsGA	ENSP00000513398.1:p.Phe6Asp
ENST00000697690.1:c.16_17delinsGA	ENSP00000513399.1:p.Phe6Asp
ENST00000697691.1:c.16_17delinsGA	ENSP00000513400.1:p.Phe6Asp
ENST00000697692.1:c.16_17delinsGA	ENSP00000513401.1:p.Phe6Asp
ENST00000337432.9:c.16_17delinsGA MANE Select	ENSP00000336701.4:p.Phe6Asp
ENST00000337432.8:c.16_17delinsGA	ENSP00000336701.4:p.Phe6Asp
ENST00000421782.3:c.16_17delinsGA	ENSP00000391450.2:p.Phe6Asp
ENST00000461271.5:c.-233_-232delinsGA	ENSP00000464056.1:n.-233_-232delinsGA
ENST00000475762.5:c.16_17delinsGA	ENSP00000432421.1:p.Phe6Asp
ENST00000476741.2:n.58_59delinsGA
ENST00000482007.5:c.16_17delinsGA	ENSP00000433332.1:p.Phe6Asp
ENST00000486827.1:c.16_17delinsGA	ENSP00000436761.1:p.Phe6Asp
ENST00000487525.5:c.16_17delinsGA	ENSP00000431637.1:p.Phe6Asp
ENST00000487921.5:n.57+27_57+28delinsGA
ENST00000583539.5:c.16_17delinsGA	ENSP00000463121.1:p.Phe6Asp
NM_002876.3:c.16_17delinsGA	NP_002867.1:p.Phe6Asp
NM_058216.2:c.16_17delinsGA	NP_478123.1:p.Phe6Asp
NR_103872.1:n.87_88delinsGA
NR_103873.1:n.87_88delinsGA
XM_006722001.2:c.16_17delinsGA	XP_006722064.1:p.Phe6Asp
XM_006722002.2:c.16_17delinsGA	XP_006722065.1:p.Phe6Asp
XM_006722004.2:c.-233_-232delinsGA	XP_006722067.1:n.-233_-232delinsGA
XM_006722005.2:c.-207+27_-207+28delinsGA	XP_006722068.1:n.-207+27_-207+28delinsGA
XM_011525092.1:c.-533_-532delinsGA	XP_011523394.1:n.-533_-532delinsGA
XM_011525093.1:c.-694_-693delinsGA	XP_011523395.1:n.-694_-693delinsGA
XR_934513.1:n.89_90delinsGA
XR_934514.1:n.89_90delinsGA
XM_006722001.4:c.16_17delinsGA	XP_006722064.1:p.Phe6Asp
XM_006722002.4:c.16_17delinsGA	XP_006722065.1:p.Phe6Asp
XM_006722004.3:c.-233_-232delinsGA	XP_006722067.1:n.-233_-232delinsGA
XM_006722005.3:c.-207+27_-207+28delinsGA	XP_006722068.1:n.-207+27_-207+28delinsGA
XM_017024914.1:c.-233_-232delinsGA	XP_016880403.1:n.-233_-232delinsGA
XM_017024916.1:c.-533_-532delinsGA	XP_016880405.1:n.-533_-532delinsGA
XM_017024917.1:c.-207+27_-207+28delinsGA	XP_016880406.1:n.-207+27_-207+28delinsGA
XM_017024918.2:c.-507_-506delinsGA	XP_016880407.1:n.-507_-506delinsGA
XR_934513.3:n.520_521delinsGA
XR_934514.3:n.520_521delinsGA
NM_058216.3:c.16_17delinsGA MANE Select	NP_478123.1:p.Phe6Asp
NR_103872.2:n.58_59delinsGA
NM_002876.4:c.16_17delinsGA	NP_002867.1:p.Phe6Asp