Canonical Allele Identifier: CA400364830

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 924258
• ClinVar RCV Id: RCV001185464 ; RCV002560871
• dbSNP Id: rs1567817289
• MyVariant Identifiers: chr17:g.56809845G>A (hg19) ; chr17:g.58732484G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732484G>A , CM000679.2:g.58732484G>A	GRCh38
NC_000017.10:g.56809845G>A , CM000679.1:g.56809845G>A	GRCh37
NC_000017.9:g.54164844G>A	NCBI36
NG_023199.1:g.44883G>A , LRG_314:g.44883G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.615G>A	ENSP00000464056.2:p.Arg205=
ENST00000697680.1:c.*1930G>A	ENSP00000513392.1:n.*1930G>A
ENST00000697681.1:c.*2127G>A	ENSP00000513393.1:n.*2127G>A
ENST00000697683.1:c.*1902G>A	ENSP00000513395.1:n.*1902G>A
ENST00000697685.1:c.*1663G>A	ENSP00000513396.1:n.*1663G>A
ENST00000697686.1:c.737G>A	ENSP00000513397.1:p.Gly246Asp
ENST00000697689.1:c.*1441-1634G>A	ENSP00000513398.1:n.*1441-1634G>A
ENST00000697690.1:c.905-1634G>A	ENSP00000513399.1:n.905-1634G>A
ENST00000697691.1:c.*938G>A	ENSP00000513400.1:n.*938G>A
ENST00000697692.1:c.*978G>A	ENSP00000513401.1:n.*978G>A
ENST00000697694.1:c.615G>A	ENSP00000513402.1:p.Arg205=
ENST00000697695.1:n.1573G>A
ENST00000337432.9:c.966G>A MANE Select	ENSP00000336701.4:p.Arg322=
ENST00000337432.8:c.966G>A	ENSP00000336701.4:p.Arg322=
ENST00000413590.5:c.607G>A
ENST00000461706.1:n.153G>A
ENST00000475762.5:c.*1602G>A	ENSP00000432421.1:n.*1602G>A
ENST00000482007.5:c.*394G>A	ENSP00000433332.1:n.*394G>A
ENST00000487525.5:c.*542G>A	ENSP00000431637.1:n.*542G>A
ENST00000578151.1:n.240-1634G>A
ENST00000581221.5:n.481G>A
ENST00000583539.5:c.966G>A	ENSP00000463121.1:p.Arg322=
ENST00000584617.5:c.688G>A
ENST00000584804.1:c.200G>A	ENSP00000463658.1:p.Gly67Asp
NM_058216.2:c.966G>A	NP_478123.1:p.Arg322=
NR_103872.1:n.870G>A
XM_006722001.2:c.969G>A	XP_006722064.1:p.Arg323=
XM_006722002.2:c.905G>A	XP_006722065.1:p.Gly302Asp
XM_006722004.2:c.618G>A	XP_006722067.1:p.Arg206=
XM_006722005.2:c.618G>A	XP_006722068.1:p.Arg206=
XM_011525092.1:c.618G>A	XP_011523394.1:p.Arg206=
XM_011525093.1:c.618G>A	XP_011523395.1:p.Arg206=
XM_011525094.1:c.618G>A	XP_011523396.1:p.Arg206=
XR_934513.1:n.1184G>A
XR_934514.1:n.1187G>A
XR_934886.1:n.149+5587C>T
XM_006722001.4:c.969G>A	XP_006722064.1:p.Arg323=
XM_006722002.4:c.905G>A	XP_006722065.1:p.Gly302Asp
XM_006722004.3:c.618G>A	XP_006722067.1:p.Arg206=
XM_006722005.3:c.618G>A	XP_006722068.1:p.Arg206=
XM_011525092.2:c.618G>A	XP_011523394.1:p.Arg206=
XM_011525093.2:c.618G>A	XP_011523395.1:p.Arg206=
XM_011525094.2:c.618G>A	XP_011523396.1:p.Arg206=
XM_017024914.1:c.615G>A	XP_016880403.1:p.Arg205=
XM_017024915.1:c.615G>A	XP_016880404.1:p.Arg205=
XM_017024916.1:c.615G>A	XP_016880405.1:p.Arg205=
XM_017024917.1:c.615G>A	XP_016880406.1:p.Arg205=
XM_017024918.2:c.615G>A	XP_016880407.1:p.Arg205=
XM_017024919.1:c.554G>A	XP_016880408.1:p.Gly185Asp
XR_934513.3:n.1615G>A
XR_934514.3:n.1618G>A
XR_934886.2:n.149+5587C>T
NM_058216.3:c.966G>A MANE Select	NP_478123.1:p.Arg322=
NR_103872.2:n.841G>A