Canonical Allele Identifier: CA501075506

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2445976
• ClinVar RCV Id: RCV003155895 ; RCV003507477
• dbSNP Id: rs2143850133
• MyVariant Identifiers: chr17:g.56787225A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709864A>T , CM000679.2:g.58709864A>T	GRCh38
NC_000017.10:g.56787225A>T , CM000679.1:g.56787225A>T	GRCh37
NC_000017.9:g.54142224A>T	NCBI36
NG_023199.1:g.22263A>T , LRG_314:g.22263A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.360A>T	ENSP00000464056.2:p.Arg120=
ENST00000697678.1:n.613A>T
ENST00000697679.1:n.1785A>T
ENST00000697680.1:c.*1575A>T	ENSP00000513392.1:n.*1575A>T
ENST00000697681.1:c.*1872A>T	ENSP00000513393.1:n.*1872A>T
ENST00000697683.1:c.*1575A>T	ENSP00000513395.1:n.*1575A>T
ENST00000697684.1:n.771A>T
ENST00000697685.1:c.*1408A>T	ENSP00000513396.1:n.*1408A>T
ENST00000697686.1:c.360A>T	ENSP00000513397.1:p.Arg120=
ENST00000697687.1:n.590A>T
ENST00000697688.1:n.757A>T
ENST00000697689.1:c.*1247A>T	ENSP00000513398.1:n.*1247A>T
ENST00000697690.1:c.711A>T	ENSP00000513399.1:p.Arg237=
ENST00000697691.1:c.*683A>T	ENSP00000513400.1:n.*683A>T
ENST00000697692.1:c.*723A>T	ENSP00000513401.1:n.*723A>T
ENST00000697694.1:c.360A>T	ENSP00000513402.1:p.Arg120=
ENST00000697695.1:n.1318A>T
ENST00000337432.9:c.711A>T MANE Select	ENSP00000336701.4:p.Arg237=
ENST00000337432.8:c.711A>T	ENSP00000336701.4:p.Arg237=
ENST00000413590.5:c.349A>T
ENST00000425173.5:c.627A>T	ENSP00000407282.1:p.Arg209=
ENST00000461271.5:c.360A>T	ENSP00000464056.1:p.Arg120=
ENST00000475762.5:c.*1414A>T	ENSP00000432421.1:n.*1414A>T
ENST00000482007.5:c.*139A>T	ENSP00000433332.1:n.*139A>T
ENST00000487525.5:c.*284A>T	ENSP00000431637.1:n.*284A>T
ENST00000578151.1:n.46A>T
ENST00000581221.5:n.226A>T
ENST00000583539.5:c.711A>T	ENSP00000463121.1:p.Arg237=
ENST00000584617.5:c.433A>T
ENST00000584804.1:c.6A>T	ENSP00000463658.1:p.Arg2=
NM_058216.2:c.711A>T	NP_478123.1:p.Arg237=
NR_103872.1:n.615A>T
XM_006722001.2:c.711A>T	XP_006722064.1:p.Arg237=
XM_006722002.2:c.711A>T	XP_006722065.1:p.Arg237=
XM_006722004.2:c.360A>T	XP_006722067.1:p.Arg120=
XM_006722005.2:c.360A>T	XP_006722068.1:p.Arg120=
XM_011525092.1:c.360A>T	XP_011523394.1:p.Arg120=
XM_011525093.1:c.360A>T	XP_011523395.1:p.Arg120=
XM_011525094.1:c.360A>T	XP_011523396.1:p.Arg120=
XR_934513.1:n.929A>T
XR_934514.1:n.929A>T
XM_006722001.4:c.711A>T	XP_006722064.1:p.Arg237=
XM_006722002.4:c.711A>T	XP_006722065.1:p.Arg237=
XM_006722004.3:c.360A>T	XP_006722067.1:p.Arg120=
XM_006722005.3:c.360A>T	XP_006722068.1:p.Arg120=
XM_011525092.2:c.360A>T	XP_011523394.1:p.Arg120=
XM_011525093.2:c.360A>T	XP_011523395.1:p.Arg120=
XM_011525094.2:c.360A>T	XP_011523396.1:p.Arg120=
XM_017024914.1:c.360A>T	XP_016880403.1:p.Arg120=
XM_017024915.1:c.360A>T	XP_016880404.1:p.Arg120=
XM_017024916.1:c.360A>T	XP_016880405.1:p.Arg120=
XM_017024917.1:c.360A>T	XP_016880406.1:p.Arg120=
XM_017024918.2:c.360A>T	XP_016880407.1:p.Arg120=
XM_017024919.1:c.360A>T	XP_016880408.1:p.Arg120=
XR_934513.3:n.1360A>T
XR_934514.3:n.1360A>T
NM_058216.3:c.711A>T MANE Select	NP_478123.1:p.Arg237=
NR_103872.2:n.586A>T