Canonical Allele Identifier: CA400349388

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2695443
• ClinVar RCV Id: RCV003507582
• dbSNP Id: rs587781921
• MyVariant Identifiers: chr17:g.56780605A>T (hg19) ; chr17:g.58703244A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703244A>T , CM000679.2:g.58703244A>T	GRCh38
NC_000017.10:g.56780605A>T , CM000679.1:g.56780605A>T	GRCh37
NC_000017.9:g.54135604A>T	NCBI36
NG_023199.1:g.15643A>T , LRG_314:g.15643A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.269A>T	ENSP00000464056.2:p.His90Leu
ENST00000697677.1:n.1701A>T
ENST00000697678.1:n.522A>T
ENST00000697679.1:n.1694A>T
ENST00000697680.1:c.*1484A>T	ENSP00000513392.1:n.*1484A>T
ENST00000697681.1:c.*1636A>T	ENSP00000513393.1:n.*1636A>T
ENST00000697683.1:c.*1484A>T	ENSP00000513395.1:n.*1484A>T
ENST00000697684.1:n.680A>T
ENST00000697685.1:c.*1317A>T	ENSP00000513396.1:n.*1317A>T
ENST00000697686.1:c.269A>T	ENSP00000513397.1:p.His90Leu
ENST00000697687.1:n.499A>T
ENST00000697688.1:n.666A>T
ENST00000697689.1:c.*1156A>T	ENSP00000513398.1:n.*1156A>T
ENST00000697690.1:c.620A>T	ENSP00000513399.1:p.His207Leu
ENST00000697691.1:c.*592A>T	ENSP00000513400.1:n.*592A>T
ENST00000697692.1:c.*632A>T	ENSP00000513401.1:n.*632A>T
ENST00000697694.1:c.269A>T	ENSP00000513402.1:p.His90Leu
ENST00000697695.1:n.1227A>T
ENST00000337432.9:c.620A>T MANE Select	ENSP00000336701.4:p.His207Leu
ENST00000337432.8:c.620A>T	ENSP00000336701.4:p.His207Leu
ENST00000413590.5:c.258A>T
ENST00000425173.5:c.416A>T	ENSP00000407282.1:p.His139Leu
ENST00000461271.5:c.269A>T	ENSP00000464056.1:p.His90Leu
ENST00000475762.5:c.*1323A>T	ENSP00000432421.1:n.*1323A>T
ENST00000482007.5:c.*48A>T	ENSP00000433332.1:n.*48A>T
ENST00000487525.5:c.*48A>T	ENSP00000431637.1:n.*48A>T
ENST00000487921.5:n.532A>T
ENST00000583539.5:c.620A>T	ENSP00000463121.1:p.His207Leu
ENST00000584617.5:c.342A>T
NM_058216.2:c.620A>T	NP_478123.1:p.His207Leu
NR_103872.1:n.524A>T
XM_006722001.2:c.620A>T	XP_006722064.1:p.His207Leu
XM_006722002.2:c.620A>T	XP_006722065.1:p.His207Leu
XM_006722004.2:c.269A>T	XP_006722067.1:p.His90Leu
XM_006722005.2:c.269A>T	XP_006722068.1:p.His90Leu
XM_011525092.1:c.269A>T	XP_011523394.1:p.His90Leu
XM_011525093.1:c.269A>T	XP_011523395.1:p.His90Leu
XM_011525094.1:c.269A>T	XP_011523396.1:p.His90Leu
XR_934513.1:n.693A>T
XR_934514.1:n.693A>T
XM_006722001.4:c.620A>T	XP_006722064.1:p.His207Leu
XM_006722002.4:c.620A>T	XP_006722065.1:p.His207Leu
XM_006722004.3:c.269A>T	XP_006722067.1:p.His90Leu
XM_006722005.3:c.269A>T	XP_006722068.1:p.His90Leu
XM_011525092.2:c.269A>T	XP_011523394.1:p.His90Leu
XM_011525093.2:c.269A>T	XP_011523395.1:p.His90Leu
XM_011525094.2:c.269A>T	XP_011523396.1:p.His90Leu
XM_017024914.1:c.269A>T	XP_016880403.1:p.His90Leu
XM_017024915.1:c.269A>T	XP_016880404.1:p.His90Leu
XM_017024916.1:c.269A>T	XP_016880405.1:p.His90Leu
XM_017024917.1:c.269A>T	XP_016880406.1:p.His90Leu
XM_017024918.2:c.269A>T	XP_016880407.1:p.His90Leu
XM_017024919.1:c.269A>T	XP_016880408.1:p.His90Leu
XR_934513.3:n.1124A>T
XR_934514.3:n.1124A>T
NM_058216.3:c.620A>T MANE Select	NP_478123.1:p.His207Leu
NR_103872.2:n.495A>T