Canonical Allele Identifier: CA501075188

Gene: RAD51C

Linked Data

• dbSNP Id: rs770096766
• MyVariant Identifiers: chr17:g.56780564A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703203A>T , CM000679.2:g.58703203A>T	GRCh38
NC_000017.10:g.56780564A>T , CM000679.1:g.56780564A>T	GRCh37
NC_000017.9:g.54135563A>T	NCBI36
NG_023199.1:g.15602A>T , LRG_314:g.15602A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.228A>T	ENSP00000464056.2:p.Arg76=
ENST00000697677.1:n.1660A>T
ENST00000697678.1:n.481A>T
ENST00000697679.1:n.1653A>T
ENST00000697680.1:c.*1443A>T	ENSP00000513392.1:n.*1443A>T
ENST00000697681.1:c.*1595A>T	ENSP00000513393.1:n.*1595A>T
ENST00000697683.1:c.*1443A>T	ENSP00000513395.1:n.*1443A>T
ENST00000697684.1:n.639A>T
ENST00000697685.1:c.*1276A>T	ENSP00000513396.1:n.*1276A>T
ENST00000697686.1:c.228A>T	ENSP00000513397.1:p.Arg76=
ENST00000697687.1:n.458A>T
ENST00000697688.1:n.625A>T
ENST00000697689.1:c.*1115A>T	ENSP00000513398.1:n.*1115A>T
ENST00000697690.1:c.579A>T	ENSP00000513399.1:p.Arg193=
ENST00000697691.1:c.*551A>T	ENSP00000513400.1:n.*551A>T
ENST00000697692.1:c.*591A>T	ENSP00000513401.1:n.*591A>T
ENST00000697694.1:c.228A>T	ENSP00000513402.1:p.Arg76=
ENST00000697695.1:n.1186A>T
ENST00000337432.9:c.579A>T MANE Select	ENSP00000336701.4:p.Arg193=
ENST00000337432.8:c.579A>T	ENSP00000336701.4:p.Arg193=
ENST00000413590.5:c.217A>T
ENST00000425173.5:c.375A>T	ENSP00000407282.1:p.Arg125=
ENST00000461271.5:c.228A>T	ENSP00000464056.1:p.Arg76=
ENST00000475762.5:c.*1282A>T	ENSP00000432421.1:n.*1282A>T
ENST00000482007.5:c.*7A>T	ENSP00000433332.1:n.*7A>T
ENST00000487525.5:c.*7A>T	ENSP00000431637.1:n.*7A>T
ENST00000487921.5:n.491A>T
ENST00000583539.5:c.579A>T	ENSP00000463121.1:p.Arg193=
ENST00000584617.5:c.301A>T
NM_058216.2:c.579A>T	NP_478123.1:p.Arg193=
NR_103872.1:n.483A>T
XM_006722001.2:c.579A>T	XP_006722064.1:p.Arg193=
XM_006722002.2:c.579A>T	XP_006722065.1:p.Arg193=
XM_006722004.2:c.228A>T	XP_006722067.1:p.Arg76=
XM_006722005.2:c.228A>T	XP_006722068.1:p.Arg76=
XM_011525092.1:c.228A>T	XP_011523394.1:p.Arg76=
XM_011525093.1:c.228A>T	XP_011523395.1:p.Arg76=
XM_011525094.1:c.228A>T	XP_011523396.1:p.Arg76=
XR_934513.1:n.652A>T
XR_934514.1:n.652A>T
XM_006722001.4:c.579A>T	XP_006722064.1:p.Arg193=
XM_006722002.4:c.579A>T	XP_006722065.1:p.Arg193=
XM_006722004.3:c.228A>T	XP_006722067.1:p.Arg76=
XM_006722005.3:c.228A>T	XP_006722068.1:p.Arg76=
XM_011525092.2:c.228A>T	XP_011523394.1:p.Arg76=
XM_011525093.2:c.228A>T	XP_011523395.1:p.Arg76=
XM_011525094.2:c.228A>T	XP_011523396.1:p.Arg76=
XM_017024914.1:c.228A>T	XP_016880403.1:p.Arg76=
XM_017024915.1:c.228A>T	XP_016880404.1:p.Arg76=
XM_017024916.1:c.228A>T	XP_016880405.1:p.Arg76=
XM_017024917.1:c.228A>T	XP_016880406.1:p.Arg76=
XM_017024918.2:c.228A>T	XP_016880407.1:p.Arg76=
XM_017024919.1:c.228A>T	XP_016880408.1:p.Arg76=
XR_934513.3:n.1083A>T
XR_934514.3:n.1083A>T
NM_058216.3:c.579A>T MANE Select	NP_478123.1:p.Arg193=
NR_103872.2:n.454A>T