Canonical Allele Identifier: CA3057228832

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692748_58692750delinsATC , CM000679.2:g.58692748_58692750delinsATC	GRCh38
NC_000017.10:g.56770109_56770111delinsATC , CM000679.1:g.56770109_56770111delinsATC	GRCh37
NC_000017.9:g.54125108_54125110delinsATC	NCBI36
NG_023199.1:g.5147_5149delinsATC , LRG_314:g.5147_5149delinsATC
NG_047169.1:g.4330_4332delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+63_-207+65delinsATC	ENSP00000464056.2:n.-207+63_-207+65delinsATC
ENST00000697675.1:n.176_178delinsATC
ENST00000697676.1:n.165_167delinsATC
ENST00000697677.1:n.163_165delinsATC
ENST00000697678.1:n.47+116_47+118delinsATC
ENST00000697679.1:n.156_158delinsATC
ENST00000697680.1:c.105_107delinsATC	ENSP00000513392.1:p.Glu36Ser
ENST00000697681.1:c.105_107delinsATC	ENSP00000513393.1:p.Glu36Ser
ENST00000697683.1:c.105_107delinsATC	ENSP00000513395.1:p.Glu36Ser
ENST00000697684.1:n.165_167delinsATC
ENST00000697685.1:c.105_107delinsATC	ENSP00000513396.1:p.Glu36Ser
ENST00000697686.1:c.-207+116_-207+118delinsATC	ENSP00000513397.1:n.-207+116_-207+118delinsATC
ENST00000697687.1:n.151_153delinsATC
ENST00000697688.1:n.151_153delinsATC
ENST00000697689.1:c.105_107delinsATC	ENSP00000513398.1:p.Glu36Ser
ENST00000697690.1:c.105_107delinsATC	ENSP00000513399.1:p.Glu36Ser
ENST00000697691.1:c.42+63_42+65delinsATC	ENSP00000513400.1:n.42+63_42+65delinsATC
ENST00000697692.1:c.105_107delinsATC	ENSP00000513401.1:p.Glu36Ser
ENST00000697693.1:n.18_20delinsATC
ENST00000337432.9:c.105_107delinsATC MANE Select	ENSP00000336701.4:p.Glu36Ser
ENST00000337432.8:c.105_107delinsATC	ENSP00000336701.4:p.Glu36Ser
ENST00000421782.3:c.105_107delinsATC	ENSP00000391450.2:p.Glu36Ser
ENST00000461271.5:c.-207+63_-207+65delinsATC	ENSP00000464056.1:n.-207+63_-207+65delinsATC
ENST00000475762.5:c.105_107delinsATC	ENSP00000432421.1:p.Glu36Ser
ENST00000476741.2:n.147_149delinsATC
ENST00000482007.5:c.105_107delinsATC	ENSP00000433332.1:p.Glu36Ser
ENST00000486827.1:c.105_107delinsATC	ENSP00000436761.1:p.Glu36Ser
ENST00000487525.5:c.105_107delinsATC	ENSP00000431637.1:p.Glu36Ser
ENST00000487921.5:n.57+116_57+118delinsATC
ENST00000583539.5:c.105_107delinsATC	ENSP00000463121.1:p.Glu36Ser
ENST00000584617.5:c.86_88delinsATC
NM_002876.3:c.105_107delinsATC	NP_002867.1:p.Glu36Ser
NM_058216.2:c.105_107delinsATC	NP_478123.1:p.Glu36Ser
NR_103872.1:n.176_178delinsATC
NR_103873.1:n.113+63_113+65delinsATC
XM_006722001.2:c.105_107delinsATC	XP_006722064.1:p.Glu36Ser
XM_006722002.2:c.105_107delinsATC	XP_006722065.1:p.Glu36Ser
XM_006722004.2:c.-207+63_-207+65delinsATC	XP_006722067.1:n.-207+63_-207+65delinsATC
XM_006722005.2:c.-207+116_-207+118delinsATC	XP_006722068.1:n.-207+116_-207+118delinsATC
XM_011525092.1:c.-507+63_-507+65delinsATC	XP_011523394.1:n.-507+63_-507+65delinsATC
XM_011525093.1:c.-668+63_-668+65delinsATC	XP_011523395.1:n.-668+63_-668+65delinsATC
XR_934513.1:n.178_180delinsATC
XR_934514.1:n.178_180delinsATC
XM_006722001.4:c.105_107delinsATC	XP_006722064.1:p.Glu36Ser
XM_006722002.4:c.105_107delinsATC	XP_006722065.1:p.Glu36Ser
XM_006722004.3:c.-207+63_-207+65delinsATC	XP_006722067.1:n.-207+63_-207+65delinsATC
XM_006722005.3:c.-207+116_-207+118delinsATC	XP_006722068.1:n.-207+116_-207+118delinsATC
XM_011525092.2:c.-507+63_-507+65delinsATC	XP_011523394.1:n.-507+63_-507+65delinsATC
XM_011525093.2:c.-668+63_-668+65delinsATC	XP_011523395.1:n.-668+63_-668+65delinsATC
XM_017024914.1:c.-207+63_-207+65delinsATC	XP_016880403.1:n.-207+63_-207+65delinsATC
XM_017024916.1:c.-507+63_-507+65delinsATC	XP_016880405.1:n.-507+63_-507+65delinsATC
XM_017024917.1:c.-207+116_-207+118delinsATC	XP_016880406.1:n.-207+116_-207+118delinsATC
XM_017024918.2:c.-418_-416delinsATC	XP_016880407.1:n.-418_-416delinsATC
XM_017024919.1:c.-668+63_-668+65delinsATC	XP_016880408.1:n.-668+63_-668+65delinsATC
XR_934513.3:n.609_611delinsATC
XR_934514.3:n.609_611delinsATC
NM_058216.3:c.105_107delinsATC MANE Select	NP_478123.1:p.Glu36Ser
NR_103872.2:n.147_149delinsATC
NM_002876.4:c.105_107delinsATC	NP_002867.1:p.Glu36Ser