Canonical Allele Identifier: CA501074337

Gene: RAD51C

Linked Data

• dbSNP Id: rs876658798
• MyVariant Identifiers: chr17:g.56770040G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692679G>T , CM000679.2:g.58692679G>T	GRCh38
NC_000017.10:g.56770040G>T , CM000679.1:g.56770040G>T	GRCh37
NC_000017.9:g.54125039G>T	NCBI36
NG_023199.1:g.5078G>T , LRG_314:g.5078G>T
NG_047169.1:g.4401C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.-213G>T	ENSP00000464056.2:n.-213G>T
ENST00000697675.1:n.107G>T
ENST00000697676.1:n.96G>T
ENST00000697677.1:n.94G>T
ENST00000697678.1:n.47+47G>T
ENST00000697679.1:n.87G>T
ENST00000697680.1:c.36G>T	ENSP00000513392.1:p.Arg12=
ENST00000697681.1:c.36G>T	ENSP00000513393.1:p.Arg12=
ENST00000697683.1:c.36G>T	ENSP00000513395.1:p.Arg12=
ENST00000697684.1:n.96G>T
ENST00000697685.1:c.36G>T	ENSP00000513396.1:p.Arg12=
ENST00000697686.1:c.-207+47G>T	ENSP00000513397.1:n.-207+47G>T
ENST00000697687.1:n.82G>T
ENST00000697688.1:n.82G>T
ENST00000697689.1:c.36G>T	ENSP00000513398.1:p.Arg12=
ENST00000697690.1:c.36G>T	ENSP00000513399.1:p.Arg12=
ENST00000697691.1:c.36G>T	ENSP00000513400.1:p.Arg12=
ENST00000697692.1:c.36G>T	ENSP00000513401.1:p.Arg12=
ENST00000337432.9:c.36G>T MANE Select	ENSP00000336701.4:p.Arg12=
ENST00000337432.8:c.36G>T	ENSP00000336701.4:p.Arg12=
ENST00000421782.3:c.36G>T	ENSP00000391450.2:p.Arg12=
ENST00000461271.5:c.-213G>T	ENSP00000464056.1:n.-213G>T
ENST00000475762.5:c.36G>T	ENSP00000432421.1:p.Arg12=
ENST00000476741.2:n.78G>T
ENST00000482007.5:c.36G>T	ENSP00000433332.1:p.Arg12=
ENST00000486827.1:c.36G>T	ENSP00000436761.1:p.Arg12=
ENST00000487525.5:c.36G>T	ENSP00000431637.1:p.Arg12=
ENST00000487921.5:n.57+47G>T
ENST00000583539.5:c.36G>T	ENSP00000463121.1:p.Arg12=
ENST00000584617.5:c.17G>T
NM_002876.3:c.36G>T	NP_002867.1:p.Arg12=
NM_058216.2:c.36G>T	NP_478123.1:p.Arg12=
NR_103872.1:n.107G>T
NR_103873.1:n.107G>T
XM_006722001.2:c.36G>T	XP_006722064.1:p.Arg12=
XM_006722002.2:c.36G>T	XP_006722065.1:p.Arg12=
XM_006722004.2:c.-213G>T	XP_006722067.1:n.-213G>T
XM_006722005.2:c.-207+47G>T	XP_006722068.1:n.-207+47G>T
XM_011525092.1:c.-513G>T	XP_011523394.1:n.-513G>T
XM_011525093.1:c.-674G>T	XP_011523395.1:n.-674G>T
XR_934513.1:n.109G>T
XR_934514.1:n.109G>T
XM_006722001.4:c.36G>T	XP_006722064.1:p.Arg12=
XM_006722002.4:c.36G>T	XP_006722065.1:p.Arg12=
XM_006722004.3:c.-213G>T	XP_006722067.1:n.-213G>T
XM_006722005.3:c.-207+47G>T	XP_006722068.1:n.-207+47G>T
XM_011525092.2:c.-513G>T	XP_011523394.1:n.-513G>T
XM_011525093.2:c.-674G>T	XP_011523395.1:n.-674G>T
XM_017024914.1:c.-213G>T	XP_016880403.1:n.-213G>T
XM_017024916.1:c.-513G>T	XP_016880405.1:n.-513G>T
XM_017024917.1:c.-207+47G>T	XP_016880406.1:n.-207+47G>T
XM_017024918.2:c.-487G>T	XP_016880407.1:n.-487G>T
XM_017024919.1:c.-674G>T	XP_016880408.1:n.-674G>T
XR_934513.3:n.540G>T
XR_934514.3:n.540G>T
NM_058216.3:c.36G>T MANE Select	NP_478123.1:p.Arg12=
NR_103872.2:n.78G>T
NM_002876.4:c.36G>T	NP_002867.1:p.Arg12=