Canonical Allele Identifier: CA3057228123

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692658_58692659delinsAG , CM000679.2:g.58692658_58692659delinsAG	GRCh38
NC_000017.10:g.56770019_56770020delinsAG , CM000679.1:g.56770019_56770020delinsAG	GRCh37
NC_000017.9:g.54125018_54125019delinsAG	NCBI36
NG_023199.1:g.5057_5058delinsAG , LRG_314:g.5057_5058delinsAG
NG_047169.1:g.4421_4422delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-234_-233delinsAG	ENSP00000464056.2:n.-234_-233delinsAG
ENST00000697675.1:n.86_87delinsAG
ENST00000697676.1:n.75_76delinsAG
ENST00000697677.1:n.73_74delinsAG
ENST00000697678.1:n.47+26_47+27delinsAG
ENST00000697679.1:n.66_67delinsAG
ENST00000697680.1:c.15_16delinsAG	ENSP00000513392.1:p.Phe6Val
ENST00000697681.1:c.15_16delinsAG	ENSP00000513393.1:p.Phe6Val
ENST00000697683.1:c.15_16delinsAG	ENSP00000513395.1:p.Phe6Val
ENST00000697684.1:n.75_76delinsAG
ENST00000697685.1:c.15_16delinsAG	ENSP00000513396.1:p.Phe6Val
ENST00000697686.1:c.-207+26_-207+27delinsAG	ENSP00000513397.1:n.-207+26_-207+27delinsAG
ENST00000697687.1:n.61_62delinsAG
ENST00000697688.1:n.61_62delinsAG
ENST00000697689.1:c.15_16delinsAG	ENSP00000513398.1:p.Phe6Val
ENST00000697690.1:c.15_16delinsAG	ENSP00000513399.1:p.Phe6Val
ENST00000697691.1:c.15_16delinsAG	ENSP00000513400.1:p.Phe6Val
ENST00000697692.1:c.15_16delinsAG	ENSP00000513401.1:p.Phe6Val
ENST00000337432.9:c.15_16delinsAG MANE Select	ENSP00000336701.4:p.Phe6Val
ENST00000337432.8:c.15_16delinsAG	ENSP00000336701.4:p.Phe6Val
ENST00000421782.3:c.15_16delinsAG	ENSP00000391450.2:p.Phe6Val
ENST00000461271.5:c.-234_-233delinsAG	ENSP00000464056.1:n.-234_-233delinsAG
ENST00000475762.5:c.15_16delinsAG	ENSP00000432421.1:p.Phe6Val
ENST00000476741.2:n.57_58delinsAG
ENST00000482007.5:c.15_16delinsAG	ENSP00000433332.1:p.Phe6Val
ENST00000486827.1:c.15_16delinsAG	ENSP00000436761.1:p.Phe6Val
ENST00000487525.5:c.15_16delinsAG	ENSP00000431637.1:p.Phe6Val
ENST00000487921.5:n.57+26_57+27delinsAG
ENST00000583539.5:c.15_16delinsAG	ENSP00000463121.1:p.Phe6Val
NM_002876.3:c.15_16delinsAG	NP_002867.1:p.Phe6Val
NM_058216.2:c.15_16delinsAG	NP_478123.1:p.Phe6Val
NR_103872.1:n.86_87delinsAG
NR_103873.1:n.86_87delinsAG
XM_006722001.2:c.15_16delinsAG	XP_006722064.1:p.Phe6Val
XM_006722002.2:c.15_16delinsAG	XP_006722065.1:p.Phe6Val
XM_006722004.2:c.-234_-233delinsAG	XP_006722067.1:n.-234_-233delinsAG
XM_006722005.2:c.-207+26_-207+27delinsAG	XP_006722068.1:n.-207+26_-207+27delinsAG
XM_011525092.1:c.-534_-533delinsAG	XP_011523394.1:n.-534_-533delinsAG
XM_011525093.1:c.-695_-694delinsAG	XP_011523395.1:n.-695_-694delinsAG
XR_934513.1:n.88_89delinsAG
XR_934514.1:n.88_89delinsAG
XM_006722001.4:c.15_16delinsAG	XP_006722064.1:p.Phe6Val
XM_006722002.4:c.15_16delinsAG	XP_006722065.1:p.Phe6Val
XM_006722004.3:c.-234_-233delinsAG	XP_006722067.1:n.-234_-233delinsAG
XM_006722005.3:c.-207+26_-207+27delinsAG	XP_006722068.1:n.-207+26_-207+27delinsAG
XM_017024914.1:c.-234_-233delinsAG	XP_016880403.1:n.-234_-233delinsAG
XM_017024916.1:c.-534_-533delinsAG	XP_016880405.1:n.-534_-533delinsAG
XM_017024917.1:c.-207+26_-207+27delinsAG	XP_016880406.1:n.-207+26_-207+27delinsAG
XM_017024918.2:c.-508_-507delinsAG	XP_016880407.1:n.-508_-507delinsAG
XR_934513.3:n.519_520delinsAG
XR_934514.3:n.519_520delinsAG
NM_058216.3:c.15_16delinsAG MANE Select	NP_478123.1:p.Phe6Val
NR_103872.2:n.57_58delinsAG
NM_002876.4:c.15_16delinsAG	NP_002867.1:p.Phe6Val