Canonical Allele Identifier: CA400336068

Gene: RAD51C

Linked Data

• dbSNP Id: rs758029117
• gnomAD v2: 17-56770008-C-A
• MyVariant Identifiers: chr17:g.56770008C>A (hg19) ; chr17:g.58692647C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58692647C>A , CM000679.2:g.58692647C>A	GRCh38
NC_000017.10:g.56770008C>A , CM000679.1:g.56770008C>A	GRCh37
NC_000017.9:g.54125007C>A	NCBI36
NG_023199.1:g.5046C>A , LRG_314:g.5046C>A
NG_047169.1:g.4433G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-245C>A	ENSP00000464056.2:n.-245C>A
ENST00000697675.1:n.75C>A
ENST00000697676.1:n.64C>A
ENST00000697677.1:n.62C>A
ENST00000697678.1:n.47+15C>A
ENST00000697679.1:n.55C>A
ENST00000697680.1:c.4C>A	ENSP00000513392.1:p.Arg2Ser
ENST00000697681.1:c.4C>A	ENSP00000513393.1:p.Arg2Ser
ENST00000697683.1:c.4C>A	ENSP00000513395.1:p.Arg2Ser
ENST00000697684.1:n.64C>A
ENST00000697685.1:c.4C>A	ENSP00000513396.1:p.Arg2Ser
ENST00000697686.1:c.-207+15C>A	ENSP00000513397.1:n.-207+15C>A
ENST00000697687.1:n.50C>A
ENST00000697688.1:n.50C>A
ENST00000697689.1:c.4C>A	ENSP00000513398.1:p.Arg2Ser
ENST00000697690.1:c.4C>A	ENSP00000513399.1:p.Arg2Ser
ENST00000697691.1:c.4C>A	ENSP00000513400.1:p.Arg2Ser
ENST00000697692.1:c.4C>A	ENSP00000513401.1:p.Arg2Ser
ENST00000337432.9:c.4C>A MANE Select	ENSP00000336701.4:p.Arg2Ser
ENST00000337432.8:c.4C>A	ENSP00000336701.4:p.Arg2Ser
ENST00000421782.3:c.4C>A	ENSP00000391450.2:p.Arg2Ser
ENST00000461271.5:c.-245C>A	ENSP00000464056.1:n.-245C>A
ENST00000475762.5:c.4C>A	ENSP00000432421.1:p.Arg2Ser
ENST00000476741.2:n.46C>A
ENST00000482007.5:c.4C>A	ENSP00000433332.1:p.Arg2Ser
ENST00000486827.1:c.4C>A	ENSP00000436761.1:p.Arg2Ser
ENST00000487525.5:c.4C>A	ENSP00000431637.1:p.Arg2Ser
ENST00000487921.5:n.57+15C>A
ENST00000583539.5:c.4C>A	ENSP00000463121.1:p.Arg2Ser
NM_002876.3:c.4C>A	NP_002867.1:p.Arg2Ser
NM_058216.2:c.4C>A	NP_478123.1:p.Arg2Ser
NR_103872.1:n.75C>A
NR_103873.1:n.75C>A
XM_006722001.2:c.4C>A	XP_006722064.1:p.Arg2Ser
XM_006722002.2:c.4C>A	XP_006722065.1:p.Arg2Ser
XM_006722004.2:c.-245C>A	XP_006722067.1:n.-245C>A
XM_006722005.2:c.-207+15C>A	XP_006722068.1:n.-207+15C>A
XM_011525092.1:c.-545C>A	XP_011523394.1:n.-545C>A
XM_011525093.1:c.-706C>A	XP_011523395.1:n.-706C>A
XR_934513.1:n.77C>A
XR_934514.1:n.77C>A
XM_006722001.4:c.4C>A	XP_006722064.1:p.Arg2Ser
XM_006722002.4:c.4C>A	XP_006722065.1:p.Arg2Ser
XM_006722004.3:c.-245C>A	XP_006722067.1:n.-245C>A
XM_006722005.3:c.-207+15C>A	XP_006722068.1:n.-207+15C>A
XM_017024914.1:c.-245C>A	XP_016880403.1:n.-245C>A
XM_017024916.1:c.-545C>A	XP_016880405.1:n.-545C>A
XM_017024917.1:c.-207+15C>A	XP_016880406.1:n.-207+15C>A
XM_017024918.2:c.-519C>A	XP_016880407.1:n.-519C>A
XR_934513.3:n.508C>A
XR_934514.3:n.508C>A
NM_058216.3:c.4C>A MANE Select	NP_478123.1:p.Arg2Ser
NR_103872.2:n.46C>A
NM_002876.4:c.4C>A	NP_002867.1:p.Arg2Ser