Canonical Allele Identifier: CA400359845

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 480510
• ClinVar RCV Id: RCV000571657 ; RCV000986014 ; RCV001047716 ; RCV003459305
• dbSNP Id: rs1555602159
• gnomAD v4: 17-58720813-G-T
• MyVariant Identifiers: chr17:g.56798174G>T (hg19) ; chr17:g.58720813G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58720813G>T , CM000679.2:g.58720813G>T	GRCh38
NC_000017.10:g.56798174G>T , CM000679.1:g.56798174G>T	GRCh37
NC_000017.9:g.54153173G>T	NCBI36
NG_023199.1:g.33212G>T , LRG_314:g.33212G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.553+1G>T	ENSP00000464056.2:n.553+1G>T
ENST00000697678.1:n.807G>T
ENST00000697679.1:n.1979G>T
ENST00000697680.1:c.*1868+1G>T	ENSP00000513392.1:n.*1868+1G>T
ENST00000697681.1:c.*2065+1G>T	ENSP00000513393.1:n.*2065+1G>T
ENST00000697683.1:c.*1768+1G>T	ENSP00000513395.1:n.*1768+1G>T
ENST00000697684.1:n.964+1G>T
ENST00000697685.1:c.*1601+1G>T	ENSP00000513396.1:n.*1601+1G>T
ENST00000697686.1:c.553+1G>T	ENSP00000513397.1:n.553+1G>T
ENST00000697687.1:n.783+1G>T
ENST00000697688.1:n.950+1G>T
ENST00000697689.1:c.*1440+1G>T	ENSP00000513398.1:n.*1440+1G>T
ENST00000697690.1:c.904+1G>T	ENSP00000513399.1:n.904+1G>T
ENST00000697691.1:c.*876+1G>T	ENSP00000513400.1:n.*876+1G>T
ENST00000697692.1:c.*916+1G>T	ENSP00000513401.1:n.*916+1G>T
ENST00000697694.1:c.553+1G>T	ENSP00000513402.1:n.553+1G>T
ENST00000697695.1:n.1511+1G>T
ENST00000337432.9:c.904+1G>T MANE Select	ENSP00000336701.4:n.904+1G>T
ENST00000337432.8:c.904+1G>T	ENSP00000336701.4:n.904+1G>T
ENST00000413590.5:c.542+1G>T
ENST00000475762.5:c.*1541-3227G>T	ENSP00000432421.1:n.*1541-3227G>T
ENST00000482007.5:c.*332+1G>T	ENSP00000433332.1:n.*332+1G>T
ENST00000487525.5:c.*477+1G>T	ENSP00000431637.1:n.*477+1G>T
ENST00000578151.1:n.239+1G>T
ENST00000581221.5:n.419+1G>T
ENST00000583539.5:c.904+1G>T	ENSP00000463121.1:n.904+1G>T
ENST00000584617.5:c.626+1G>T
ENST00000584804.1:c.199+1G>T	ENSP00000463658.1:n.199+1G>T
NM_058216.2:c.904+1G>T	NP_478123.1:n.904+1G>T
NR_103872.1:n.808+1G>T
XM_006722001.2:c.904+1G>T	XP_006722064.1:n.904+1G>T
XM_006722002.2:c.904+1G>T	XP_006722065.1:n.904+1G>T
XM_006722004.2:c.553+1G>T	XP_006722067.1:n.553+1G>T
XM_006722005.2:c.553+1G>T	XP_006722068.1:n.553+1G>T
XM_011525092.1:c.553+1G>T	XP_011523394.1:n.553+1G>T
XM_011525093.1:c.553+1G>T	XP_011523395.1:n.553+1G>T
XM_011525094.1:c.553+1G>T	XP_011523396.1:n.553+1G>T
XR_934513.1:n.1122+1G>T
XR_934514.1:n.1122+1G>T
XM_006722001.4:c.904+1G>T	XP_006722064.1:n.904+1G>T
XM_006722002.4:c.904+1G>T	XP_006722065.1:n.904+1G>T
XM_006722004.3:c.553+1G>T	XP_006722067.1:n.553+1G>T
XM_006722005.3:c.553+1G>T	XP_006722068.1:n.553+1G>T
XM_011525092.2:c.553+1G>T	XP_011523394.1:n.553+1G>T
XM_011525093.2:c.553+1G>T	XP_011523395.1:n.553+1G>T
XM_011525094.2:c.553+1G>T	XP_011523396.1:n.553+1G>T
XM_017024914.1:c.553+1G>T	XP_016880403.1:n.553+1G>T
XM_017024915.1:c.553+1G>T	XP_016880404.1:n.553+1G>T
XM_017024916.1:c.553+1G>T	XP_016880405.1:n.553+1G>T
XM_017024917.1:c.553+1G>T	XP_016880406.1:n.553+1G>T
XM_017024918.2:c.553+1G>T	XP_016880407.1:n.553+1G>T
XM_017024919.1:c.553+1G>T	XP_016880408.1:n.553+1G>T
XR_934513.3:n.1553+1G>T
XR_934514.3:n.1553+1G>T
NM_058216.3:c.904+1G>T MANE Select	NP_478123.1:n.904+1G>T
NR_103872.2:n.779+1G>T