Canonical Allele Identifier: CA16615468

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 409846
• ClinVar RCV Id: RCV000464529 ; RCV002411483
• dbSNP Id: rs1060502590
• MyVariant Identifiers: chr17:g.56811512G>A (hg19) ; chr17:g.58734151G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58734151G>A , CM000679.2:g.58734151G>A	GRCh38
NC_000017.10:g.56811512G>A , CM000679.1:g.56811512G>A	GRCh37
NC_000017.9:g.54166511G>A	NCBI36
NG_023199.1:g.46550G>A , LRG_314:g.46550G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.*1592G>A	ENSP00000464056.2:n.*1592G>A
ENST00000697680.1:c.*2024G>A	ENSP00000513392.1:n.*2024G>A
ENST00000697681.1:c.*2221G>A	ENSP00000513393.1:n.*2221G>A
ENST00000697683.1:c.*1996G>A	ENSP00000513395.1:n.*1996G>A
ENST00000697685.1:c.*1757G>A	ENSP00000513396.1:n.*1757G>A
ENST00000697686.1:c.831G>A	ENSP00000513397.1:p.Leu277=
ENST00000697689.1:c.*1474G>A	ENSP00000513398.1:n.*1474G>A
ENST00000697690.1:c.*20G>A	ENSP00000513399.1:n.*20G>A
ENST00000697691.1:c.*1032G>A	ENSP00000513400.1:n.*1032G>A
ENST00000697692.1:c.*1072G>A	ENSP00000513401.1:n.*1072G>A
ENST00000697694.1:c.709G>A	ENSP00000513402.1:p.Ala237Thr
ENST00000697695.1:n.1667G>A
ENST00000337432.9:c.1060G>A MANE Select	ENSP00000336701.4:p.Ala354Thr
ENST00000337432.8:c.1060G>A	ENSP00000336701.4:p.Ala354Thr
ENST00000413590.5:c.701G>A
ENST00000461706.1:n.247G>A
ENST00000475762.5:c.*1696G>A	ENSP00000432421.1:n.*1696G>A
ENST00000482007.5:c.*488G>A	ENSP00000433332.1:n.*488G>A
ENST00000487525.5:c.*636G>A	ENSP00000431637.1:n.*636G>A
ENST00000578151.1:n.273G>A
ENST00000581221.5:n.575G>A
ENST00000584804.1:c.294G>A	ENSP00000463658.1:p.Leu98=
NM_058216.2:c.1060G>A	NP_478123.1:p.Ala354Thr
NR_103872.1:n.964G>A
XM_006722001.2:c.1063G>A	XP_006722064.1:p.Ala355Thr
XM_006722002.2:c.999G>A	XP_006722065.1:p.Leu333=
XM_006722004.2:c.712G>A	XP_006722067.1:p.Ala238Thr
XM_006722005.2:c.712G>A	XP_006722068.1:p.Ala238Thr
XM_011525092.1:c.712G>A	XP_011523394.1:p.Ala238Thr
XM_011525093.1:c.712G>A	XP_011523395.1:p.Ala238Thr
XM_011525094.1:c.712G>A	XP_011523396.1:p.Ala238Thr
XR_934513.1:n.1278G>A
XR_934514.1:n.1281G>A
XR_934886.1:n.149+3920C>T
XM_006722001.4:c.1063G>A	XP_006722064.1:p.Ala355Thr
XM_006722002.4:c.999G>A	XP_006722065.1:p.Leu333=
XM_006722004.3:c.712G>A	XP_006722067.1:p.Ala238Thr
XM_006722005.3:c.712G>A	XP_006722068.1:p.Ala238Thr
XM_011525092.2:c.712G>A	XP_011523394.1:p.Ala238Thr
XM_011525093.2:c.712G>A	XP_011523395.1:p.Ala238Thr
XM_011525094.2:c.712G>A	XP_011523396.1:p.Ala238Thr
XM_017024914.1:c.709G>A	XP_016880403.1:p.Ala237Thr
XM_017024915.1:c.709G>A	XP_016880404.1:p.Ala237Thr
XM_017024916.1:c.709G>A	XP_016880405.1:p.Ala237Thr
XM_017024917.1:c.709G>A	XP_016880406.1:p.Ala237Thr
XM_017024918.2:c.709G>A	XP_016880407.1:p.Ala237Thr
XM_017024919.1:c.648G>A	XP_016880408.1:p.Leu216=
XR_934513.3:n.1709G>A
XR_934514.3:n.1712G>A
XR_934886.2:n.149+3920C>T
NM_058216.3:c.1060G>A MANE Select	NP_478123.1:p.Ala354Thr
NR_103872.2:n.935G>A