Canonical Allele Identifier: CA348863

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 220140
• ClinVar RCV Id: RCV000204660 ; RCV000213392 ; RCV000780666 ; RCV001762438 ; RCV003468942
• dbSNP Id: rs864622395
• gnomAD v4: 17-58724095-G-C
• MyVariant Identifiers: chr17:g.56801456G>C (hg19) ; chr17:g.58724095G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724095G>C , CM000679.2:g.58724095G>C	GRCh38
NC_000017.10:g.56801456G>C , CM000679.1:g.56801456G>C	GRCh37
NC_000017.9:g.54156455G>C	NCBI36
NG_023199.1:g.36494G>C , LRG_314:g.36494G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.609G>C	ENSP00000464056.2:p.Lys203Asn
ENST00000697680.1:c.*1924G>C	ENSP00000513392.1:n.*1924G>C
ENST00000697681.1:c.*2121G>C	ENSP00000513393.1:n.*2121G>C
ENST00000697683.1:c.*1824G>C	ENSP00000513395.1:n.*1824G>C
ENST00000697684.1:n.1020G>C
ENST00000697685.1:c.*1657G>C	ENSP00000513396.1:n.*1657G>C
ENST00000697686.1:c.609G>C	ENSP00000513397.1:p.Lys203Asn
ENST00000697687.1:n.839G>C
ENST00000697688.1:n.1006G>C
ENST00000697689.1:c.*1440+3283G>C	ENSP00000513398.1:n.*1440+3283G>C
ENST00000697690.1:c.904+3283G>C	ENSP00000513399.1:n.904+3283G>C
ENST00000697691.1:c.*932G>C	ENSP00000513400.1:n.*932G>C
ENST00000697692.1:c.*972G>C	ENSP00000513401.1:n.*972G>C
ENST00000697694.1:c.609G>C	ENSP00000513402.1:p.Lys203Asn
ENST00000697695.1:n.1567G>C
ENST00000337432.9:c.960G>C MANE Select	ENSP00000336701.4:p.Lys320Asn
ENST00000337432.8:c.960G>C	ENSP00000336701.4:p.Lys320Asn
ENST00000413590.5:c.598G>C
ENST00000475762.5:c.*1596G>C	ENSP00000432421.1:n.*1596G>C
ENST00000482007.5:c.*388G>C	ENSP00000433332.1:n.*388G>C
ENST00000487525.5:c.*533G>C	ENSP00000431637.1:n.*533G>C
ENST00000578151.1:n.239+3283G>C
ENST00000581221.5:n.475G>C
ENST00000583539.5:c.960G>C	ENSP00000463121.1:p.Lys320Asn
ENST00000584617.5:c.682G>C
ENST00000584804.1:c.199+3283G>C	ENSP00000463658.1:n.199+3283G>C
NM_058216.2:c.960G>C	NP_478123.1:p.Lys320Asn
NR_103872.1:n.864G>C
XM_006722001.2:c.960G>C	XP_006722064.1:p.Lys320Asn
XM_006722002.2:c.904+3283G>C	XP_006722065.1:n.904+3283G>C
XM_006722004.2:c.609G>C	XP_006722067.1:p.Lys203Asn
XM_006722005.2:c.609G>C	XP_006722068.1:p.Lys203Asn
XM_011525092.1:c.609G>C	XP_011523394.1:p.Lys203Asn
XM_011525093.1:c.609G>C	XP_011523395.1:p.Lys203Asn
XM_011525094.1:c.609G>C	XP_011523396.1:p.Lys203Asn
XR_934513.1:n.1178G>C
XR_934514.1:n.1178G>C
XM_006722001.4:c.960G>C	XP_006722064.1:p.Lys320Asn
XM_006722002.4:c.904+3283G>C	XP_006722065.1:n.904+3283G>C
XM_006722004.3:c.609G>C	XP_006722067.1:p.Lys203Asn
XM_006722005.3:c.609G>C	XP_006722068.1:p.Lys203Asn
XM_011525092.2:c.609G>C	XP_011523394.1:p.Lys203Asn
XM_011525093.2:c.609G>C	XP_011523395.1:p.Lys203Asn
XM_011525094.2:c.609G>C	XP_011523396.1:p.Lys203Asn
XM_017024914.1:c.609G>C	XP_016880403.1:p.Lys203Asn
XM_017024915.1:c.609G>C	XP_016880404.1:p.Lys203Asn
XM_017024916.1:c.609G>C	XP_016880405.1:p.Lys203Asn
XM_017024917.1:c.609G>C	XP_016880406.1:p.Lys203Asn
XM_017024918.2:c.609G>C	XP_016880407.1:p.Lys203Asn
XM_017024919.1:c.553+3283G>C	XP_016880408.1:n.553+3283G>C
XR_934513.3:n.1609G>C
XR_934514.3:n.1609G>C
NM_058216.3:c.960G>C MANE Select	NP_478123.1:p.Lys320Asn
NR_103872.2:n.835G>C