Canonical Allele Identifier: CA400353357

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56787245T>G (hg19) ; chr17:g.58709884T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709884T>G , CM000679.2:g.58709884T>G	GRCh38
NC_000017.10:g.56787245T>G , CM000679.1:g.56787245T>G	GRCh37
NC_000017.9:g.54142244T>G	NCBI36
NG_023199.1:g.22283T>G , LRG_314:g.22283T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.380T>G	ENSP00000464056.2:p.Ile127Ser
ENST00000697678.1:n.633T>G
ENST00000697679.1:n.1805T>G
ENST00000697680.1:c.*1595T>G	ENSP00000513392.1:n.*1595T>G
ENST00000697681.1:c.*1892T>G	ENSP00000513393.1:n.*1892T>G
ENST00000697683.1:c.*1595T>G	ENSP00000513395.1:n.*1595T>G
ENST00000697684.1:n.791T>G
ENST00000697685.1:c.*1428T>G	ENSP00000513396.1:n.*1428T>G
ENST00000697686.1:c.380T>G	ENSP00000513397.1:p.Ile127Ser
ENST00000697687.1:n.610T>G
ENST00000697688.1:n.777T>G
ENST00000697689.1:c.*1267T>G	ENSP00000513398.1:n.*1267T>G
ENST00000697690.1:c.731T>G	ENSP00000513399.1:p.Ile244Ser
ENST00000697691.1:c.*703T>G	ENSP00000513400.1:n.*703T>G
ENST00000697692.1:c.*743T>G	ENSP00000513401.1:n.*743T>G
ENST00000697694.1:c.380T>G	ENSP00000513402.1:p.Ile127Ser
ENST00000697695.1:n.1338T>G
ENST00000337432.9:c.731T>G MANE Select	ENSP00000336701.4:p.Ile244Ser
ENST00000337432.8:c.731T>G	ENSP00000336701.4:p.Ile244Ser
ENST00000413590.5:c.369T>G
ENST00000461271.5:c.380T>G	ENSP00000464056.1:p.Ile127Ser
ENST00000475762.5:c.*1434T>G	ENSP00000432421.1:n.*1434T>G
ENST00000482007.5:c.*159T>G	ENSP00000433332.1:n.*159T>G
ENST00000487525.5:c.*304T>G	ENSP00000431637.1:n.*304T>G
ENST00000578151.1:n.66T>G
ENST00000581221.5:n.246T>G
ENST00000583539.5:c.731T>G	ENSP00000463121.1:p.Ile244Ser
ENST00000584617.5:c.453T>G
ENST00000584804.1:c.26T>G	ENSP00000463658.1:p.Ile9Ser
NM_058216.2:c.731T>G	NP_478123.1:p.Ile244Ser
NR_103872.1:n.635T>G
XM_006722001.2:c.731T>G	XP_006722064.1:p.Ile244Ser
XM_006722002.2:c.731T>G	XP_006722065.1:p.Ile244Ser
XM_006722004.2:c.380T>G	XP_006722067.1:p.Ile127Ser
XM_006722005.2:c.380T>G	XP_006722068.1:p.Ile127Ser
XM_011525092.1:c.380T>G	XP_011523394.1:p.Ile127Ser
XM_011525093.1:c.380T>G	XP_011523395.1:p.Ile127Ser
XM_011525094.1:c.380T>G	XP_011523396.1:p.Ile127Ser
XR_934513.1:n.949T>G
XR_934514.1:n.949T>G
XM_006722001.4:c.731T>G	XP_006722064.1:p.Ile244Ser
XM_006722002.4:c.731T>G	XP_006722065.1:p.Ile244Ser
XM_006722004.3:c.380T>G	XP_006722067.1:p.Ile127Ser
XM_006722005.3:c.380T>G	XP_006722068.1:p.Ile127Ser
XM_011525092.2:c.380T>G	XP_011523394.1:p.Ile127Ser
XM_011525093.2:c.380T>G	XP_011523395.1:p.Ile127Ser
XM_011525094.2:c.380T>G	XP_011523396.1:p.Ile127Ser
XM_017024914.1:c.380T>G	XP_016880403.1:p.Ile127Ser
XM_017024915.1:c.380T>G	XP_016880404.1:p.Ile127Ser
XM_017024916.1:c.380T>G	XP_016880405.1:p.Ile127Ser
XM_017024917.1:c.380T>G	XP_016880406.1:p.Ile127Ser
XM_017024918.2:c.380T>G	XP_016880407.1:p.Ile127Ser
XM_017024919.1:c.380T>G	XP_016880408.1:p.Ile127Ser
XR_934513.3:n.1380T>G
XR_934514.3:n.1380T>G
NM_058216.3:c.731T>G MANE Select	NP_478123.1:p.Ile244Ser
NR_103872.2:n.606T>G