Canonical Allele Identifier: CA3057228218

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692740_58692741delinsGG , CM000679.2:g.58692740_58692741delinsGG	GRCh38
NC_000017.10:g.56770101_56770102delinsGG , CM000679.1:g.56770101_56770102delinsGG	GRCh37
NC_000017.9:g.54125100_54125101delinsGG	NCBI36
NG_023199.1:g.5139_5140delinsGG , LRG_314:g.5139_5140delinsGG
NG_047169.1:g.4339_4340delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-207+55_-207+56delinsGG	ENSP00000464056.2:n.-207+55_-207+56delinsGG
ENST00000697675.1:n.168_169delinsGG
ENST00000697676.1:n.157_158delinsGG
ENST00000697677.1:n.155_156delinsGG
ENST00000697678.1:n.47+108_47+109delinsGG
ENST00000697679.1:n.148_149delinsGG
ENST00000697680.1:c.97_98delinsGG	ENSP00000513392.1:p.Gln33Gly
ENST00000697681.1:c.97_98delinsGG	ENSP00000513393.1:p.Gln33Gly
ENST00000697683.1:c.97_98delinsGG	ENSP00000513395.1:p.Gln33Gly
ENST00000697684.1:n.157_158delinsGG
ENST00000697685.1:c.97_98delinsGG	ENSP00000513396.1:p.Gln33Gly
ENST00000697686.1:c.-207+108_-207+109delinsGG	ENSP00000513397.1:n.-207+108_-207+109delinsGG
ENST00000697687.1:n.143_144delinsGG
ENST00000697688.1:n.143_144delinsGG
ENST00000697689.1:c.97_98delinsGG	ENSP00000513398.1:p.Gln33Gly
ENST00000697690.1:c.97_98delinsGG	ENSP00000513399.1:p.Gln33Gly
ENST00000697691.1:c.42+55_42+56delinsGG	ENSP00000513400.1:n.42+55_42+56delinsGG
ENST00000697692.1:c.97_98delinsGG	ENSP00000513401.1:p.Gln33Gly
ENST00000697693.1:n.10_11delinsGG
ENST00000337432.9:c.97_98delinsGG MANE Select	ENSP00000336701.4:p.Gln33Gly
ENST00000337432.8:c.97_98delinsGG	ENSP00000336701.4:p.Gln33Gly
ENST00000421782.3:c.97_98delinsGG	ENSP00000391450.2:p.Gln33Gly
ENST00000461271.5:c.-207+55_-207+56delinsGG	ENSP00000464056.1:n.-207+55_-207+56delinsGG
ENST00000475762.5:c.97_98delinsGG	ENSP00000432421.1:p.Gln33Gly
ENST00000476741.2:n.139_140delinsGG
ENST00000482007.5:c.97_98delinsGG	ENSP00000433332.1:p.Gln33Gly
ENST00000486827.1:c.97_98delinsGG	ENSP00000436761.1:p.Gln33Gly
ENST00000487525.5:c.97_98delinsGG	ENSP00000431637.1:p.Gln33Gly
ENST00000487921.5:n.57+108_57+109delinsGG
ENST00000583539.5:c.97_98delinsGG	ENSP00000463121.1:p.Gln33Gly
ENST00000584617.5:c.78_79delinsGG
NM_002876.3:c.97_98delinsGG	NP_002867.1:p.Gln33Gly
NM_058216.2:c.97_98delinsGG	NP_478123.1:p.Gln33Gly
NR_103872.1:n.168_169delinsGG
NR_103873.1:n.113+55_113+56delinsGG
XM_006722001.2:c.97_98delinsGG	XP_006722064.1:p.Gln33Gly
XM_006722002.2:c.97_98delinsGG	XP_006722065.1:p.Gln33Gly
XM_006722004.2:c.-207+55_-207+56delinsGG	XP_006722067.1:n.-207+55_-207+56delinsGG
XM_006722005.2:c.-207+108_-207+109delinsGG	XP_006722068.1:n.-207+108_-207+109delinsGG
XM_011525092.1:c.-507+55_-507+56delinsGG	XP_011523394.1:n.-507+55_-507+56delinsGG
XM_011525093.1:c.-668+55_-668+56delinsGG	XP_011523395.1:n.-668+55_-668+56delinsGG
XR_934513.1:n.170_171delinsGG
XR_934514.1:n.170_171delinsGG
XM_006722001.4:c.97_98delinsGG	XP_006722064.1:p.Gln33Gly
XM_006722002.4:c.97_98delinsGG	XP_006722065.1:p.Gln33Gly
XM_006722004.3:c.-207+55_-207+56delinsGG	XP_006722067.1:n.-207+55_-207+56delinsGG
XM_006722005.3:c.-207+108_-207+109delinsGG	XP_006722068.1:n.-207+108_-207+109delinsGG
XM_011525092.2:c.-507+55_-507+56delinsGG	XP_011523394.1:n.-507+55_-507+56delinsGG
XM_011525093.2:c.-668+55_-668+56delinsGG	XP_011523395.1:n.-668+55_-668+56delinsGG
XM_017024914.1:c.-207+55_-207+56delinsGG	XP_016880403.1:n.-207+55_-207+56delinsGG
XM_017024916.1:c.-507+55_-507+56delinsGG	XP_016880405.1:n.-507+55_-507+56delinsGG
XM_017024917.1:c.-207+108_-207+109delinsGG	XP_016880406.1:n.-207+108_-207+109delinsGG
XM_017024918.2:c.-426_-425delinsGG	XP_016880407.1:n.-426_-425delinsGG
XM_017024919.1:c.-668+55_-668+56delinsGG	XP_016880408.1:n.-668+55_-668+56delinsGG
XR_934513.3:n.601_602delinsGG
XR_934514.3:n.601_602delinsGG
NM_058216.3:c.97_98delinsGG MANE Select	NP_478123.1:p.Gln33Gly
NR_103872.2:n.139_140delinsGG
NM_002876.4:c.97_98delinsGG	NP_002867.1:p.Gln33Gly