Canonical Allele Identifier: CA400349143

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 538770
• ClinVar RCV Id: RCV000648231 ; RCV003465411
• dbSNP Id: rs1555597094
• MyVariant Identifiers: chr17:g.56780574G>T (hg19) ; chr17:g.58703213G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703213G>T , CM000679.2:g.58703213G>T	GRCh38
NC_000017.10:g.56780574G>T , CM000679.1:g.56780574G>T	GRCh37
NC_000017.9:g.54135573G>T	NCBI36
NG_023199.1:g.15612G>T , LRG_314:g.15612G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.238G>T	ENSP00000464056.2:p.Glu80Ter
ENST00000697677.1:n.1670G>T
ENST00000697678.1:n.491G>T
ENST00000697679.1:n.1663G>T
ENST00000697680.1:c.*1453G>T	ENSP00000513392.1:n.*1453G>T
ENST00000697681.1:c.*1605G>T	ENSP00000513393.1:n.*1605G>T
ENST00000697683.1:c.*1453G>T	ENSP00000513395.1:n.*1453G>T
ENST00000697684.1:n.649G>T
ENST00000697685.1:c.*1286G>T	ENSP00000513396.1:n.*1286G>T
ENST00000697686.1:c.238G>T	ENSP00000513397.1:p.Glu80Ter
ENST00000697687.1:n.468G>T
ENST00000697688.1:n.635G>T
ENST00000697689.1:c.*1125G>T	ENSP00000513398.1:n.*1125G>T
ENST00000697690.1:c.589G>T	ENSP00000513399.1:p.Glu197Ter
ENST00000697691.1:c.*561G>T	ENSP00000513400.1:n.*561G>T
ENST00000697692.1:c.*601G>T	ENSP00000513401.1:n.*601G>T
ENST00000697694.1:c.238G>T	ENSP00000513402.1:p.Glu80Ter
ENST00000697695.1:n.1196G>T
ENST00000337432.9:c.589G>T MANE Select	ENSP00000336701.4:p.Glu197Ter
ENST00000337432.8:c.589G>T	ENSP00000336701.4:p.Glu197Ter
ENST00000413590.5:c.227G>T
ENST00000425173.5:c.385G>T	ENSP00000407282.1:p.Glu129Ter
ENST00000461271.5:c.238G>T	ENSP00000464056.1:p.Glu80Ter
ENST00000475762.5:c.*1292G>T	ENSP00000432421.1:n.*1292G>T
ENST00000482007.5:c.*17G>T	ENSP00000433332.1:n.*17G>T
ENST00000487525.5:c.*17G>T	ENSP00000431637.1:n.*17G>T
ENST00000487921.5:n.501G>T
ENST00000583539.5:c.589G>T	ENSP00000463121.1:p.Glu197Ter
ENST00000584617.5:c.311G>T
NM_058216.2:c.589G>T	NP_478123.1:p.Glu197Ter
NR_103872.1:n.493G>T
XM_006722001.2:c.589G>T	XP_006722064.1:p.Glu197Ter
XM_006722002.2:c.589G>T	XP_006722065.1:p.Glu197Ter
XM_006722004.2:c.238G>T	XP_006722067.1:p.Glu80Ter
XM_006722005.2:c.238G>T	XP_006722068.1:p.Glu80Ter
XM_011525092.1:c.238G>T	XP_011523394.1:p.Glu80Ter
XM_011525093.1:c.238G>T	XP_011523395.1:p.Glu80Ter
XM_011525094.1:c.238G>T	XP_011523396.1:p.Glu80Ter
XR_934513.1:n.662G>T
XR_934514.1:n.662G>T
XM_006722001.4:c.589G>T	XP_006722064.1:p.Glu197Ter
XM_006722002.4:c.589G>T	XP_006722065.1:p.Glu197Ter
XM_006722004.3:c.238G>T	XP_006722067.1:p.Glu80Ter
XM_006722005.3:c.238G>T	XP_006722068.1:p.Glu80Ter
XM_011525092.2:c.238G>T	XP_011523394.1:p.Glu80Ter
XM_011525093.2:c.238G>T	XP_011523395.1:p.Glu80Ter
XM_011525094.2:c.238G>T	XP_011523396.1:p.Glu80Ter
XM_017024914.1:c.238G>T	XP_016880403.1:p.Glu80Ter
XM_017024915.1:c.238G>T	XP_016880404.1:p.Glu80Ter
XM_017024916.1:c.238G>T	XP_016880405.1:p.Glu80Ter
XM_017024917.1:c.238G>T	XP_016880406.1:p.Glu80Ter
XM_017024918.2:c.238G>T	XP_016880407.1:p.Glu80Ter
XM_017024919.1:c.238G>T	XP_016880408.1:p.Glu80Ter
XR_934513.3:n.1093G>T
XR_934514.3:n.1093G>T
NM_058216.3:c.589G>T MANE Select	NP_478123.1:p.Glu197Ter
NR_103872.2:n.464G>T