Canonical Allele Identifier: CA3057228152

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692685_58692687delinsAGC , CM000679.2:g.58692685_58692687delinsAGC	GRCh38
NC_000017.10:g.56770046_56770048delinsAGC , CM000679.1:g.56770046_56770048delinsAGC	GRCh37
NC_000017.9:g.54125045_54125047delinsAGC	NCBI36
NG_023199.1:g.5084_5086delinsAGC , LRG_314:g.5084_5086delinsAGC
NG_047169.1:g.4393_4395delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.42_44delinsAGC MANE Select	NP_478123.1:p.Val15Ala
ENST00000337432.9:c.42_44delinsAGC MANE Select	ENSP00000336701.4:p.Val15Ala
NM_002876.3:c.42_44delinsAGC	NP_002867.1:p.Val15Ala
NM_002876.4:c.42_44delinsAGC	NP_002867.1:p.Val15Ala
NM_058216.2:c.42_44delinsAGC	NP_478123.1:p.Val15Ala
NR_103872.1:n.113_115delinsAGC
NR_103872.2:n.84_86delinsAGC
NR_103873.1:n.113_113+2delinsAGC
ENST00000337432.8:c.42_44delinsAGC	ENSP00000336701.4:p.Val15Ala
ENST00000421782.3:c.42_44delinsAGC	ENSP00000391450.2:p.Val15Ala
ENST00000461271.5:c.-207_-207+2delinsAGC
ENST00000461271.6:c.-207_-207+2delinsAGC
ENST00000475762.5:c.42_44delinsAGC	ENSP00000432421.1:p.Val15Ala
ENST00000476741.2:n.84_86delinsAGC
ENST00000482007.5:c.42_44delinsAGC	ENSP00000433332.1:p.Val15Ala
ENST00000486827.1:c.42_44delinsAGC	ENSP00000436761.1:p.Val15Ala
ENST00000487525.5:c.42_44delinsAGC	ENSP00000431637.1:p.Val15Ala
ENST00000487921.5:n.57+53_57+55delinsAGC
ENST00000583539.5:c.42_44delinsAGC	ENSP00000463121.1:p.Val15Ala
ENST00000584617.5:c.23_25delinsAGC
ENST00000697675.1:n.113_115delinsAGC
ENST00000697676.1:n.102_104delinsAGC
ENST00000697677.1:n.100_102delinsAGC
ENST00000697678.1:n.47+53_47+55delinsAGC
ENST00000697679.1:n.93_95delinsAGC
ENST00000697680.1:c.42_44delinsAGC	ENSP00000513392.1:p.Val15Ala
ENST00000697681.1:c.42_44delinsAGC	ENSP00000513393.1:p.Val15Ala
ENST00000697683.1:c.42_44delinsAGC	ENSP00000513395.1:p.Val15Ala
ENST00000697684.1:n.102_104delinsAGC
ENST00000697685.1:c.42_44delinsAGC	ENSP00000513396.1:p.Val15Ala
ENST00000697686.1:c.-207+53_-207+55delinsAGC	ENSP00000513397.1:n.-207+53_-207+55delinsAGC
ENST00000697687.1:n.88_90delinsAGC
ENST00000697688.1:n.88_90delinsAGC
ENST00000697689.1:c.42_44delinsAGC	ENSP00000513398.1:p.Val15Ala
ENST00000697690.1:c.42_44delinsAGC	ENSP00000513399.1:p.Val15Ala
ENST00000697691.1:c.42_42+2delinsAGC
ENST00000697692.1:c.42_44delinsAGC	ENSP00000513401.1:p.Val15Ala
XM_006722001.2:c.42_44delinsAGC	XP_006722064.1:p.Val15Ala
XM_006722001.4:c.42_44delinsAGC	XP_006722064.1:p.Val15Ala
XM_006722002.2:c.42_44delinsAGC	XP_006722065.1:p.Val15Ala
XM_006722002.4:c.42_44delinsAGC	XP_006722065.1:p.Val15Ala
XM_006722004.2:c.-207_-207+2delinsAGC
XM_006722004.3:c.-207_-207+2delinsAGC
XM_006722005.2:c.-207+53_-207+55delinsAGC	XP_006722068.1:n.-207+53_-207+55delinsAGC
XM_006722005.3:c.-207+53_-207+55delinsAGC	XP_006722068.1:n.-207+53_-207+55delinsAGC
XM_011525092.1:c.-507_-507+2delinsAGC
XM_011525092.2:c.-507_-507+2delinsAGC
XM_011525093.1:c.-668_-668+2delinsAGC
XM_011525093.2:c.-668_-668+2delinsAGC
XM_017024914.1:c.-207_-207+2delinsAGC
XM_017024916.1:c.-507_-507+2delinsAGC
XM_017024917.1:c.-207+53_-207+55delinsAGC	XP_016880406.1:n.-207+53_-207+55delinsAGC
XM_017024918.2:c.-481_-479delinsAGC	XP_016880407.1:n.-481_-479delinsAGC
XM_017024919.1:c.-668_-668+2delinsAGC
XR_934513.1:n.115_117delinsAGC
XR_934513.3:n.546_548delinsAGC
XR_934514.1:n.115_117delinsAGC
XR_934514.3:n.546_548delinsAGC