Canonical Allele Identifier: CA400361406

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1443174
• ClinVar RCV Id: RCV001953368
• dbSNP Id: rs786203766
• MyVariant Identifiers: chr17:g.56801428T>A (hg19) ; chr17:g.58724067T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724067T>A , CM000679.2:g.58724067T>A	GRCh38
NC_000017.10:g.56801428T>A , CM000679.1:g.56801428T>A	GRCh37
NC_000017.9:g.54156427T>A	NCBI36
NG_023199.1:g.36466T>A , LRG_314:g.36466T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.581T>A	ENSP00000464056.2:p.Ile194Lys
ENST00000697680.1:c.*1896T>A	ENSP00000513392.1:n.*1896T>A
ENST00000697681.1:c.*2093T>A	ENSP00000513393.1:n.*2093T>A
ENST00000697683.1:c.*1796T>A	ENSP00000513395.1:n.*1796T>A
ENST00000697684.1:n.992T>A
ENST00000697685.1:c.*1629T>A	ENSP00000513396.1:n.*1629T>A
ENST00000697686.1:c.581T>A	ENSP00000513397.1:p.Ile194Lys
ENST00000697687.1:n.811T>A
ENST00000697688.1:n.978T>A
ENST00000697689.1:c.*1440+3255T>A	ENSP00000513398.1:n.*1440+3255T>A
ENST00000697690.1:c.904+3255T>A	ENSP00000513399.1:n.904+3255T>A
ENST00000697691.1:c.*904T>A	ENSP00000513400.1:n.*904T>A
ENST00000697692.1:c.*944T>A	ENSP00000513401.1:n.*944T>A
ENST00000697694.1:c.581T>A	ENSP00000513402.1:p.Ile194Lys
ENST00000697695.1:n.1539T>A
ENST00000337432.9:c.932T>A MANE Select	ENSP00000336701.4:p.Ile311Lys
ENST00000337432.8:c.932T>A	ENSP00000336701.4:p.Ile311Lys
ENST00000413590.5:c.570T>A
ENST00000475762.5:c.*1568T>A	ENSP00000432421.1:n.*1568T>A
ENST00000482007.5:c.*360T>A	ENSP00000433332.1:n.*360T>A
ENST00000487525.5:c.*505T>A	ENSP00000431637.1:n.*505T>A
ENST00000578151.1:n.239+3255T>A
ENST00000581221.5:n.447T>A
ENST00000583539.5:c.932T>A	ENSP00000463121.1:p.Ile311Lys
ENST00000584617.5:c.654T>A
ENST00000584804.1:c.199+3255T>A	ENSP00000463658.1:n.199+3255T>A
NM_058216.2:c.932T>A	NP_478123.1:p.Ile311Lys
NR_103872.1:n.836T>A
XM_006722001.2:c.932T>A	XP_006722064.1:p.Ile311Lys
XM_006722002.2:c.904+3255T>A	XP_006722065.1:n.904+3255T>A
XM_006722004.2:c.581T>A	XP_006722067.1:p.Ile194Lys
XM_006722005.2:c.581T>A	XP_006722068.1:p.Ile194Lys
XM_011525092.1:c.581T>A	XP_011523394.1:p.Ile194Lys
XM_011525093.1:c.581T>A	XP_011523395.1:p.Ile194Lys
XM_011525094.1:c.581T>A	XP_011523396.1:p.Ile194Lys
XR_934513.1:n.1150T>A
XR_934514.1:n.1150T>A
XM_006722001.4:c.932T>A	XP_006722064.1:p.Ile311Lys
XM_006722002.4:c.904+3255T>A	XP_006722065.1:n.904+3255T>A
XM_006722004.3:c.581T>A	XP_006722067.1:p.Ile194Lys
XM_006722005.3:c.581T>A	XP_006722068.1:p.Ile194Lys
XM_011525092.2:c.581T>A	XP_011523394.1:p.Ile194Lys
XM_011525093.2:c.581T>A	XP_011523395.1:p.Ile194Lys
XM_011525094.2:c.581T>A	XP_011523396.1:p.Ile194Lys
XM_017024914.1:c.581T>A	XP_016880403.1:p.Ile194Lys
XM_017024915.1:c.581T>A	XP_016880404.1:p.Ile194Lys
XM_017024916.1:c.581T>A	XP_016880405.1:p.Ile194Lys
XM_017024917.1:c.581T>A	XP_016880406.1:p.Ile194Lys
XM_017024918.2:c.581T>A	XP_016880407.1:p.Ile194Lys
XM_017024919.1:c.553+3255T>A	XP_016880408.1:n.553+3255T>A
XR_934513.3:n.1581T>A
XR_934514.3:n.1581T>A
NM_058216.3:c.932T>A MANE Select	NP_478123.1:p.Ile311Lys
NR_103872.2:n.807T>A