Canonical Allele Identifier: CA3057228223

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692740_58692741delinsAT , CM000679.2:g.58692740_58692741delinsAT	GRCh38
NC_000017.10:g.56770101_56770102delinsAT , CM000679.1:g.56770101_56770102delinsAT	GRCh37
NC_000017.9:g.54125100_54125101delinsAT	NCBI36
NG_023199.1:g.5139_5140delinsAT , LRG_314:g.5139_5140delinsAT
NG_047169.1:g.4339_4340delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+55_-207+56delinsAT	ENSP00000464056.2:n.-207+55_-207+56delinsAT
ENST00000697675.1:n.168_169delinsAT
ENST00000697676.1:n.157_158delinsAT
ENST00000697677.1:n.155_156delinsAT
ENST00000697678.1:n.47+108_47+109delinsAT
ENST00000697679.1:n.148_149delinsAT
ENST00000697680.1:c.97_98delinsAT	ENSP00000513392.1:p.Gln33Met
ENST00000697681.1:c.97_98delinsAT	ENSP00000513393.1:p.Gln33Met
ENST00000697683.1:c.97_98delinsAT	ENSP00000513395.1:p.Gln33Met
ENST00000697684.1:n.157_158delinsAT
ENST00000697685.1:c.97_98delinsAT	ENSP00000513396.1:p.Gln33Met
ENST00000697686.1:c.-207+108_-207+109delinsAT	ENSP00000513397.1:n.-207+108_-207+109delinsAT
ENST00000697687.1:n.143_144delinsAT
ENST00000697688.1:n.143_144delinsAT
ENST00000697689.1:c.97_98delinsAT	ENSP00000513398.1:p.Gln33Met
ENST00000697690.1:c.97_98delinsAT	ENSP00000513399.1:p.Gln33Met
ENST00000697691.1:c.42+55_42+56delinsAT	ENSP00000513400.1:n.42+55_42+56delinsAT
ENST00000697692.1:c.97_98delinsAT	ENSP00000513401.1:p.Gln33Met
ENST00000697693.1:n.10_11delinsAT
ENST00000337432.9:c.97_98delinsAT MANE Select	ENSP00000336701.4:p.Gln33Met
ENST00000337432.8:c.97_98delinsAT	ENSP00000336701.4:p.Gln33Met
ENST00000421782.3:c.97_98delinsAT	ENSP00000391450.2:p.Gln33Met
ENST00000461271.5:c.-207+55_-207+56delinsAT	ENSP00000464056.1:n.-207+55_-207+56delinsAT
ENST00000475762.5:c.97_98delinsAT	ENSP00000432421.1:p.Gln33Met
ENST00000476741.2:n.139_140delinsAT
ENST00000482007.5:c.97_98delinsAT	ENSP00000433332.1:p.Gln33Met
ENST00000486827.1:c.97_98delinsAT	ENSP00000436761.1:p.Gln33Met
ENST00000487525.5:c.97_98delinsAT	ENSP00000431637.1:p.Gln33Met
ENST00000487921.5:n.57+108_57+109delinsAT
ENST00000583539.5:c.97_98delinsAT	ENSP00000463121.1:p.Gln33Met
ENST00000584617.5:c.78_79delinsAT
NM_002876.3:c.97_98delinsAT	NP_002867.1:p.Gln33Met
NM_058216.2:c.97_98delinsAT	NP_478123.1:p.Gln33Met
NR_103872.1:n.168_169delinsAT
NR_103873.1:n.113+55_113+56delinsAT
XM_006722001.2:c.97_98delinsAT	XP_006722064.1:p.Gln33Met
XM_006722002.2:c.97_98delinsAT	XP_006722065.1:p.Gln33Met
XM_006722004.2:c.-207+55_-207+56delinsAT	XP_006722067.1:n.-207+55_-207+56delinsAT
XM_006722005.2:c.-207+108_-207+109delinsAT	XP_006722068.1:n.-207+108_-207+109delinsAT
XM_011525092.1:c.-507+55_-507+56delinsAT	XP_011523394.1:n.-507+55_-507+56delinsAT
XM_011525093.1:c.-668+55_-668+56delinsAT	XP_011523395.1:n.-668+55_-668+56delinsAT
XR_934513.1:n.170_171delinsAT
XR_934514.1:n.170_171delinsAT
XM_006722001.4:c.97_98delinsAT	XP_006722064.1:p.Gln33Met
XM_006722002.4:c.97_98delinsAT	XP_006722065.1:p.Gln33Met
XM_006722004.3:c.-207+55_-207+56delinsAT	XP_006722067.1:n.-207+55_-207+56delinsAT
XM_006722005.3:c.-207+108_-207+109delinsAT	XP_006722068.1:n.-207+108_-207+109delinsAT
XM_011525092.2:c.-507+55_-507+56delinsAT	XP_011523394.1:n.-507+55_-507+56delinsAT
XM_011525093.2:c.-668+55_-668+56delinsAT	XP_011523395.1:n.-668+55_-668+56delinsAT
XM_017024914.1:c.-207+55_-207+56delinsAT	XP_016880403.1:n.-207+55_-207+56delinsAT
XM_017024916.1:c.-507+55_-507+56delinsAT	XP_016880405.1:n.-507+55_-507+56delinsAT
XM_017024917.1:c.-207+108_-207+109delinsAT	XP_016880406.1:n.-207+108_-207+109delinsAT
XM_017024918.2:c.-426_-425delinsAT	XP_016880407.1:n.-426_-425delinsAT
XM_017024919.1:c.-668+55_-668+56delinsAT	XP_016880408.1:n.-668+55_-668+56delinsAT
XR_934513.3:n.601_602delinsAT
XR_934514.3:n.601_602delinsAT
NM_058216.3:c.97_98delinsAT MANE Select	NP_478123.1:p.Gln33Met
NR_103872.2:n.139_140delinsAT
NM_002876.4:c.97_98delinsAT	NP_002867.1:p.Gln33Met