Canonical Allele Identifier: CA400342149

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56772549T>A (hg19) ; chr17:g.58695188T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58695188T>A , CM000679.2:g.58695188T>A	GRCh38
NC_000017.10:g.56772549T>A , CM000679.1:g.56772549T>A	GRCh37
NC_000017.9:g.54127548T>A	NCBI36
NG_023199.1:g.7587T>A , LRG_314:g.7587T>A
NG_047169.1:g.1892A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.52T>A	ENSP00000464056.2:p.Cys18Ser
ENST00000697675.1:n.1497T>A
ENST00000697676.1:n.463T>A
ENST00000697677.1:n.1484T>A
ENST00000697678.1:n.305T>A
ENST00000697679.1:n.1477T>A
ENST00000697680.1:c.*1267T>A	ENSP00000513392.1:n.*1267T>A
ENST00000697681.1:c.*1267T>A	ENSP00000513393.1:n.*1267T>A
ENST00000697683.1:c.*1267T>A	ENSP00000513395.1:n.*1267T>A
ENST00000697684.1:n.463T>A
ENST00000697685.1:c.*1267T>A	ENSP00000513396.1:n.*1267T>A
ENST00000697686.1:c.52T>A	ENSP00000513397.1:p.Cys18Ser
ENST00000697687.1:n.449T>A
ENST00000697688.1:n.449T>A
ENST00000697689.1:c.*1106T>A	ENSP00000513398.1:n.*1106T>A
ENST00000697690.1:c.403T>A	ENSP00000513399.1:p.Cys135Ser
ENST00000697691.1:c.*375T>A	ENSP00000513400.1:n.*375T>A
ENST00000697692.1:c.*415T>A	ENSP00000513401.1:n.*415T>A
ENST00000697693.1:n.1178T>A
ENST00000697694.1:c.52T>A	ENSP00000513402.1:p.Cys18Ser
ENST00000697695.1:n.1010T>A
ENST00000337432.9:c.403T>A MANE Select	ENSP00000336701.4:p.Cys135Ser
ENST00000337432.8:c.403T>A	ENSP00000336701.4:p.Cys135Ser
ENST00000413590.5:c.41T>A
ENST00000421782.3:c.403T>A	ENSP00000391450.2:p.Trp135Arg
ENST00000425173.5:c.199T>A	ENSP00000407282.1:p.Cys67Ser
ENST00000461271.5:c.52T>A	ENSP00000464056.1:p.Cys18Ser
ENST00000475762.5:c.*1106T>A	ENSP00000432421.1:n.*1106T>A
ENST00000482007.5:c.403T>A	ENSP00000433332.1:p.Ter135Arg
ENST00000486827.1:c.*1267T>A	ENSP00000436761.1:n.*1267T>A
ENST00000487525.5:c.403T>A	ENSP00000431637.1:p.Ter135Arg
ENST00000487921.5:n.315T>A
ENST00000583539.5:c.403T>A	ENSP00000463121.1:p.Cys135Ser
ENST00000584617.5:c.127-1505T>A
ENST00000622327.4:c.139T>A	ENSP00000482326.1:p.Cys47Ser
NM_002876.3:c.403T>A	NP_002867.1:p.Trp135Arg
NM_058216.2:c.403T>A	NP_478123.1:p.Cys135Ser
NR_103872.1:n.474T>A
NR_103873.1:n.371T>A
XM_006722001.2:c.403T>A	XP_006722064.1:p.Cys135Ser
XM_006722002.2:c.403T>A	XP_006722065.1:p.Cys135Ser
XM_006722004.2:c.52T>A	XP_006722067.1:p.Cys18Ser
XM_006722005.2:c.52T>A	XP_006722068.1:p.Cys18Ser
XM_011525092.1:c.52T>A	XP_011523394.1:p.Cys18Ser
XM_011525093.1:c.52T>A	XP_011523395.1:p.Cys18Ser
XM_011525094.1:c.52T>A	XP_011523396.1:p.Cys18Ser
XR_934513.1:n.476T>A
XR_934514.1:n.476T>A
XM_006722001.4:c.403T>A	XP_006722064.1:p.Cys135Ser
XM_006722002.4:c.403T>A	XP_006722065.1:p.Cys135Ser
XM_006722004.3:c.52T>A	XP_006722067.1:p.Cys18Ser
XM_006722005.3:c.52T>A	XP_006722068.1:p.Cys18Ser
XM_011525092.2:c.52T>A	XP_011523394.1:p.Cys18Ser
XM_011525093.2:c.52T>A	XP_011523395.1:p.Cys18Ser
XM_011525094.2:c.52T>A	XP_011523396.1:p.Cys18Ser
XM_017024914.1:c.52T>A	XP_016880403.1:p.Cys18Ser
XM_017024915.1:c.52T>A	XP_016880404.1:p.Cys18Ser
XM_017024916.1:c.52T>A	XP_016880405.1:p.Cys18Ser
XM_017024917.1:c.52T>A	XP_016880406.1:p.Cys18Ser
XM_017024918.2:c.52T>A	XP_016880407.1:p.Cys18Ser
XM_017024919.1:c.52T>A	XP_016880408.1:p.Cys18Ser
XR_934513.3:n.907T>A
XR_934514.3:n.907T>A
NM_058216.3:c.403T>A MANE Select	NP_478123.1:p.Cys135Ser
NR_103872.2:n.445T>A
NM_002876.4:c.403T>A	NP_002867.1:p.Trp135Arg