Canonical Allele Identifier: CA501075907

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1171207
• ClinVar RCV Id: RCV001524151 ; RCV002070302
• dbSNP Id: rs2143961955
• gnomAD v4: 17-58724062-T-C
• MyVariant Identifiers: chr17:g.56801423T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724062T>C , CM000679.2:g.58724062T>C	GRCh38
NC_000017.10:g.56801423T>C , CM000679.1:g.56801423T>C	GRCh37
NC_000017.9:g.54156422T>C	NCBI36
NG_023199.1:g.36461T>C , LRG_314:g.36461T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.576T>C	ENSP00000464056.2:p.Ala192=
ENST00000697680.1:c.*1891T>C	ENSP00000513392.1:n.*1891T>C
ENST00000697681.1:c.*2088T>C	ENSP00000513393.1:n.*2088T>C
ENST00000697683.1:c.*1791T>C	ENSP00000513395.1:n.*1791T>C
ENST00000697684.1:n.987T>C
ENST00000697685.1:c.*1624T>C	ENSP00000513396.1:n.*1624T>C
ENST00000697686.1:c.576T>C	ENSP00000513397.1:p.Ala192=
ENST00000697687.1:n.806T>C
ENST00000697688.1:n.973T>C
ENST00000697689.1:c.*1440+3250T>C	ENSP00000513398.1:n.*1440+3250T>C
ENST00000697690.1:c.904+3250T>C	ENSP00000513399.1:n.904+3250T>C
ENST00000697691.1:c.*899T>C	ENSP00000513400.1:n.*899T>C
ENST00000697692.1:c.*939T>C	ENSP00000513401.1:n.*939T>C
ENST00000697694.1:c.576T>C	ENSP00000513402.1:p.Ala192=
ENST00000697695.1:n.1534T>C
ENST00000337432.9:c.927T>C MANE Select	ENSP00000336701.4:p.Ala309=
ENST00000337432.8:c.927T>C	ENSP00000336701.4:p.Ala309=
ENST00000413590.5:c.565T>C
ENST00000475762.5:c.*1563T>C	ENSP00000432421.1:n.*1563T>C
ENST00000482007.5:c.*355T>C	ENSP00000433332.1:n.*355T>C
ENST00000487525.5:c.*500T>C	ENSP00000431637.1:n.*500T>C
ENST00000578151.1:n.239+3250T>C
ENST00000581221.5:n.442T>C
ENST00000583539.5:c.927T>C	ENSP00000463121.1:p.Ala309=
ENST00000584617.5:c.649T>C
ENST00000584804.1:c.199+3250T>C	ENSP00000463658.1:n.199+3250T>C
NM_058216.2:c.927T>C	NP_478123.1:p.Ala309=
NR_103872.1:n.831T>C
XM_006722001.2:c.927T>C	XP_006722064.1:p.Ala309=
XM_006722002.2:c.904+3250T>C	XP_006722065.1:n.904+3250T>C
XM_006722004.2:c.576T>C	XP_006722067.1:p.Ala192=
XM_006722005.2:c.576T>C	XP_006722068.1:p.Ala192=
XM_011525092.1:c.576T>C	XP_011523394.1:p.Ala192=
XM_011525093.1:c.576T>C	XP_011523395.1:p.Ala192=
XM_011525094.1:c.576T>C	XP_011523396.1:p.Ala192=
XR_934513.1:n.1145T>C
XR_934514.1:n.1145T>C
XM_006722001.4:c.927T>C	XP_006722064.1:p.Ala309=
XM_006722002.4:c.904+3250T>C	XP_006722065.1:n.904+3250T>C
XM_006722004.3:c.576T>C	XP_006722067.1:p.Ala192=
XM_006722005.3:c.576T>C	XP_006722068.1:p.Ala192=
XM_011525092.2:c.576T>C	XP_011523394.1:p.Ala192=
XM_011525093.2:c.576T>C	XP_011523395.1:p.Ala192=
XM_011525094.2:c.576T>C	XP_011523396.1:p.Ala192=
XM_017024914.1:c.576T>C	XP_016880403.1:p.Ala192=
XM_017024915.1:c.576T>C	XP_016880404.1:p.Ala192=
XM_017024916.1:c.576T>C	XP_016880405.1:p.Ala192=
XM_017024917.1:c.576T>C	XP_016880406.1:p.Ala192=
XM_017024918.2:c.576T>C	XP_016880407.1:p.Ala192=
XM_017024919.1:c.553+3250T>C	XP_016880408.1:n.553+3250T>C
XR_934513.3:n.1576T>C
XR_934514.3:n.1576T>C
NM_058216.3:c.927T>C MANE Select	NP_478123.1:p.Ala309=
NR_103872.2:n.802T>C