Canonical Allele Identifier: CA8677183

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 482168
• ClinVar RCV Id: RCV000565395 ; RCV000801716 ; RCV001779013 ; RCV003962628
• dbSNP Id: rs770335248
• ExAC: 17:56772336 A / T
• gnomAD v2: 17-56772336-A-T
• gnomAD v4: 17-58694975-A-T
• MyVariant Identifiers: chr17:g.56772336A>T (hg19) ; chr17:g.58694975A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694975A>T , CM000679.2:g.58694975A>T	GRCh38
NC_000017.10:g.56772336A>T , CM000679.1:g.56772336A>T	GRCh37
NC_000017.9:g.54127335A>T	NCBI36
NG_023199.1:g.7374A>T , LRG_314:g.7374A>T
NG_047169.1:g.2105T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-162A>T	ENSP00000464056.2:n.-162A>T
ENST00000697675.1:n.1284A>T
ENST00000697676.1:n.250A>T
ENST00000697677.1:n.1271A>T
ENST00000697678.1:n.92A>T
ENST00000697679.1:n.1264A>T
ENST00000697680.1:c.*1054A>T	ENSP00000513392.1:n.*1054A>T
ENST00000697681.1:c.*1054A>T	ENSP00000513393.1:n.*1054A>T
ENST00000697683.1:c.*1054A>T	ENSP00000513395.1:n.*1054A>T
ENST00000697684.1:n.250A>T
ENST00000697685.1:c.*1054A>T	ENSP00000513396.1:n.*1054A>T
ENST00000697686.1:c.-162A>T	ENSP00000513397.1:n.-162A>T
ENST00000697687.1:n.236A>T
ENST00000697688.1:n.236A>T
ENST00000697689.1:c.*893A>T	ENSP00000513398.1:n.*893A>T
ENST00000697690.1:c.190A>T	ENSP00000513399.1:p.Ile64Phe
ENST00000697691.1:c.*162A>T	ENSP00000513400.1:n.*162A>T
ENST00000697692.1:c.*202A>T	ENSP00000513401.1:n.*202A>T
ENST00000697693.1:n.965A>T
ENST00000697694.1:c.-162A>T	ENSP00000513402.1:n.-162A>T
ENST00000697695.1:n.797A>T
ENST00000337432.9:c.190A>T MANE Select	ENSP00000336701.4:p.Ile64Phe
ENST00000337432.8:c.190A>T	ENSP00000336701.4:p.Ile64Phe
ENST00000421782.3:c.190A>T	ENSP00000391450.2:p.Ile64Phe
ENST00000461271.5:c.-162A>T	ENSP00000464056.1:n.-162A>T
ENST00000475762.5:c.*893A>T	ENSP00000432421.1:n.*893A>T
ENST00000482007.5:c.190A>T	ENSP00000433332.1:p.Ile64Phe
ENST00000486827.1:c.*1054A>T	ENSP00000436761.1:n.*1054A>T
ENST00000487525.5:c.190A>T	ENSP00000431637.1:p.Ile64Phe
ENST00000487921.5:n.102A>T
ENST00000583539.5:c.190A>T	ENSP00000463121.1:p.Ile64Phe
ENST00000584617.5:c.127-1718A>T
NM_002876.3:c.190A>T	NP_002867.1:p.Ile64Phe
NM_058216.2:c.190A>T	NP_478123.1:p.Ile64Phe
NR_103872.1:n.261A>T
NR_103873.1:n.158A>T
XM_006722001.2:c.190A>T	XP_006722064.1:p.Ile64Phe
XM_006722002.2:c.190A>T	XP_006722065.1:p.Ile64Phe
XM_006722004.2:c.-162A>T	XP_006722067.1:n.-162A>T
XM_006722005.2:c.-162A>T	XP_006722068.1:n.-162A>T
XM_011525092.1:c.-162A>T	XP_011523394.1:n.-162A>T
XM_011525093.1:c.-162A>T	XP_011523395.1:n.-162A>T
XM_011525094.1:c.-162A>T	XP_011523396.1:n.-162A>T
XR_934513.1:n.263A>T
XR_934514.1:n.263A>T
XM_006722001.4:c.190A>T	XP_006722064.1:p.Ile64Phe
XM_006722002.4:c.190A>T	XP_006722065.1:p.Ile64Phe
XM_006722004.3:c.-162A>T	XP_006722067.1:n.-162A>T
XM_006722005.3:c.-162A>T	XP_006722068.1:n.-162A>T
XM_011525092.2:c.-162A>T	XP_011523394.1:n.-162A>T
XM_011525093.2:c.-162A>T	XP_011523395.1:n.-162A>T
XM_011525094.2:c.-162A>T	XP_011523396.1:n.-162A>T
XM_017024914.1:c.-162A>T	XP_016880403.1:n.-162A>T
XM_017024915.1:c.-162A>T	XP_016880404.1:n.-162A>T
XM_017024916.1:c.-162A>T	XP_016880405.1:n.-162A>T
XM_017024917.1:c.-162A>T	XP_016880406.1:n.-162A>T
XM_017024918.2:c.-162A>T	XP_016880407.1:n.-162A>T
XM_017024919.1:c.-162A>T	XP_016880408.1:n.-162A>T
XR_934513.3:n.694A>T
XR_934514.3:n.694A>T
NM_058216.3:c.190A>T MANE Select	NP_478123.1:p.Ile64Phe
NR_103872.2:n.232A>T
NM_002876.4:c.190A>T	NP_002867.1:p.Ile64Phe