Canonical Allele Identifier: CA2638989829

Gene: RAD51C

Linked Data

• gnomAD v4: 17-58694974-T-TA

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-162dup	ENSP00000464056.2:n.-162dup
ENST00000697675.1:n.1284dup
ENST00000697676.1:n.250dup
ENST00000697677.1:n.1271dup
ENST00000697678.1:n.92dup
ENST00000697679.1:n.1264dup
ENST00000697680.1:c.*1054dup	ENSP00000513392.1:n.*1054dup
ENST00000697681.1:c.*1054dup	ENSP00000513393.1:n.*1054dup
ENST00000697683.1:c.*1054dup	ENSP00000513395.1:n.*1054dup
ENST00000697684.1:n.250dup
ENST00000697685.1:c.*1054dup	ENSP00000513396.1:n.*1054dup
ENST00000697686.1:c.-162dup	ENSP00000513397.1:n.-162dup
ENST00000697687.1:n.236dup
ENST00000697688.1:n.236dup
ENST00000697689.1:c.*893dup	ENSP00000513398.1:n.*893dup
ENST00000697690.1:c.190dup	ENSP00000513399.1:p.Ile64AsnfsTer9
ENST00000697691.1:c.*162dup	ENSP00000513400.1:n.*162dup
ENST00000697692.1:c.*202dup	ENSP00000513401.1:n.*202dup
ENST00000697693.1:n.965dup
ENST00000697694.1:c.-162dup	ENSP00000513402.1:n.-162dup
ENST00000697695.1:n.797dup
ENST00000337432.9:c.190dup MANE Select	ENSP00000336701.4:p.Ile64AsnfsTer9
ENST00000337432.8:c.190dup	ENSP00000336701.4:p.Ile64AsnfsTer9
ENST00000421782.3:c.190dup	ENSP00000391450.2:p.Ile64AsnfsTer9
ENST00000461271.5:c.-162dup	ENSP00000464056.1:n.-162dup
ENST00000475762.5:c.*893dup	ENSP00000432421.1:n.*893dup
ENST00000482007.5:c.190dup	ENSP00000433332.1:p.Ile64AsnfsTer9
ENST00000486827.1:c.*1054dup	ENSP00000436761.1:n.*1054dup
ENST00000487525.5:c.190dup	ENSP00000431637.1:p.Ile64AsnfsTer9
ENST00000487921.5:n.102dup
ENST00000583539.5:c.190dup	ENSP00000463121.1:p.Ile64AsnfsTer9
ENST00000584617.5:c.127-1718dup
NM_002876.3:c.190dup	NP_002867.1:p.Ile64AsnfsTer9
NM_058216.2:c.190dup	NP_478123.1:p.Ile64AsnfsTer9
NR_103872.1:n.261dup
NR_103873.1:n.158dup
XM_006722001.2:c.190dup	XP_006722064.1:p.Ile64AsnfsTer9
XM_006722002.2:c.190dup	XP_006722065.1:p.Ile64AsnfsTer9
XM_006722004.2:c.-162dup	XP_006722067.1:n.-162dup
XM_006722005.2:c.-162dup	XP_006722068.1:n.-162dup
XM_011525092.1:c.-162dup	XP_011523394.1:n.-162dup
XM_011525093.1:c.-162dup	XP_011523395.1:n.-162dup
XM_011525094.1:c.-162dup	XP_011523396.1:n.-162dup
XR_934513.1:n.263dup
XR_934514.1:n.263dup
XM_006722001.4:c.190dup	XP_006722064.1:p.Ile64AsnfsTer9
XM_006722002.4:c.190dup	XP_006722065.1:p.Ile64AsnfsTer9
XM_006722004.3:c.-162dup	XP_006722067.1:n.-162dup
XM_006722005.3:c.-162dup	XP_006722068.1:n.-162dup
XM_011525092.2:c.-162dup	XP_011523394.1:n.-162dup
XM_011525093.2:c.-162dup	XP_011523395.1:n.-162dup
XM_011525094.2:c.-162dup	XP_011523396.1:n.-162dup
XM_017024914.1:c.-162dup	XP_016880403.1:n.-162dup
XM_017024915.1:c.-162dup	XP_016880404.1:n.-162dup
XM_017024916.1:c.-162dup	XP_016880405.1:n.-162dup
XM_017024917.1:c.-162dup	XP_016880406.1:n.-162dup
XM_017024918.2:c.-162dup	XP_016880407.1:n.-162dup
XM_017024919.1:c.-162dup	XP_016880408.1:n.-162dup
XR_934513.3:n.694dup
XR_934514.3:n.694dup
NM_058216.3:c.190dup MANE Select	NP_478123.1:p.Ile64AsnfsTer9
NR_103872.2:n.232dup
NM_002876.4:c.190dup	NP_002867.1:p.Ile64AsnfsTer9