Canonical Allele Identifier: CA3057228116

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692650_58692651delinsAT , CM000679.2:g.58692650_58692651delinsAT	GRCh38
NC_000017.10:g.56770011_56770012delinsAT , CM000679.1:g.56770011_56770012delinsAT	GRCh37
NC_000017.9:g.54125010_54125011delinsAT	NCBI36
NG_023199.1:g.5049_5050delinsAT , LRG_314:g.5049_5050delinsAT
NG_047169.1:g.4429_4430delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-242_-241delinsAT	ENSP00000464056.2:n.-242_-241delinsAT
ENST00000697675.1:n.78_79delinsAT
ENST00000697676.1:n.67_68delinsAT
ENST00000697677.1:n.65_66delinsAT
ENST00000697678.1:n.47+18_47+19delinsAT
ENST00000697679.1:n.58_59delinsAT
ENST00000697680.1:c.7_8delinsAT	ENSP00000513392.1:p.Gly3Met
ENST00000697681.1:c.7_8delinsAT	ENSP00000513393.1:p.Gly3Met
ENST00000697683.1:c.7_8delinsAT	ENSP00000513395.1:p.Gly3Met
ENST00000697684.1:n.67_68delinsAT
ENST00000697685.1:c.7_8delinsAT	ENSP00000513396.1:p.Gly3Met
ENST00000697686.1:c.-207+18_-207+19delinsAT	ENSP00000513397.1:n.-207+18_-207+19delinsAT
ENST00000697687.1:n.53_54delinsAT
ENST00000697688.1:n.53_54delinsAT
ENST00000697689.1:c.7_8delinsAT	ENSP00000513398.1:p.Gly3Met
ENST00000697690.1:c.7_8delinsAT	ENSP00000513399.1:p.Gly3Met
ENST00000697691.1:c.7_8delinsAT	ENSP00000513400.1:p.Gly3Met
ENST00000697692.1:c.7_8delinsAT	ENSP00000513401.1:p.Gly3Met
ENST00000337432.9:c.7_8delinsAT MANE Select	ENSP00000336701.4:p.Gly3Met
ENST00000337432.8:c.7_8delinsAT	ENSP00000336701.4:p.Gly3Met
ENST00000421782.3:c.7_8delinsAT	ENSP00000391450.2:p.Gly3Met
ENST00000461271.5:c.-242_-241delinsAT	ENSP00000464056.1:n.-242_-241delinsAT
ENST00000475762.5:c.7_8delinsAT	ENSP00000432421.1:p.Gly3Met
ENST00000476741.2:n.49_50delinsAT
ENST00000482007.5:c.7_8delinsAT	ENSP00000433332.1:p.Gly3Met
ENST00000486827.1:c.7_8delinsAT	ENSP00000436761.1:p.Gly3Met
ENST00000487525.5:c.7_8delinsAT	ENSP00000431637.1:p.Gly3Met
ENST00000487921.5:n.57+18_57+19delinsAT
ENST00000583539.5:c.7_8delinsAT	ENSP00000463121.1:p.Gly3Met
NM_002876.3:c.7_8delinsAT	NP_002867.1:p.Gly3Met
NM_058216.2:c.7_8delinsAT	NP_478123.1:p.Gly3Met
NR_103872.1:n.78_79delinsAT
NR_103873.1:n.78_79delinsAT
XM_006722001.2:c.7_8delinsAT	XP_006722064.1:p.Gly3Met
XM_006722002.2:c.7_8delinsAT	XP_006722065.1:p.Gly3Met
XM_006722004.2:c.-242_-241delinsAT	XP_006722067.1:n.-242_-241delinsAT
XM_006722005.2:c.-207+18_-207+19delinsAT	XP_006722068.1:n.-207+18_-207+19delinsAT
XM_011525092.1:c.-542_-541delinsAT	XP_011523394.1:n.-542_-541delinsAT
XM_011525093.1:c.-703_-702delinsAT	XP_011523395.1:n.-703_-702delinsAT
XR_934513.1:n.80_81delinsAT
XR_934514.1:n.80_81delinsAT
XM_006722001.4:c.7_8delinsAT	XP_006722064.1:p.Gly3Met
XM_006722002.4:c.7_8delinsAT	XP_006722065.1:p.Gly3Met
XM_006722004.3:c.-242_-241delinsAT	XP_006722067.1:n.-242_-241delinsAT
XM_006722005.3:c.-207+18_-207+19delinsAT	XP_006722068.1:n.-207+18_-207+19delinsAT
XM_017024914.1:c.-242_-241delinsAT	XP_016880403.1:n.-242_-241delinsAT
XM_017024916.1:c.-542_-541delinsAT	XP_016880405.1:n.-542_-541delinsAT
XM_017024917.1:c.-207+18_-207+19delinsAT	XP_016880406.1:n.-207+18_-207+19delinsAT
XM_017024918.2:c.-516_-515delinsAT	XP_016880407.1:n.-516_-515delinsAT
XR_934513.3:n.511_512delinsAT
XR_934514.3:n.511_512delinsAT
NM_058216.3:c.7_8delinsAT MANE Select	NP_478123.1:p.Gly3Met
NR_103872.2:n.49_50delinsAT
NM_002876.4:c.7_8delinsAT	NP_002867.1:p.Gly3Met