Canonical Allele Identifier: CA400354286

Gene: RAD51C

Linked Data

• dbSNP Id: rs376853755
• MyVariant Identifiers: chr17:g.56787327C>G (hg19) ; chr17:g.58709966C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709966C>G , CM000679.2:g.58709966C>G	GRCh38
NC_000017.10:g.56787327C>G , CM000679.1:g.56787327C>G	GRCh37
NC_000017.9:g.54142326C>G	NCBI36
NG_023199.1:g.22365C>G , LRG_314:g.22365C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.462C>G	ENSP00000464056.2:p.Ser154Arg
ENST00000697678.1:n.715C>G
ENST00000697679.1:n.1887C>G
ENST00000697680.1:c.*1677C>G	ENSP00000513392.1:n.*1677C>G
ENST00000697681.1:c.*1974C>G	ENSP00000513393.1:n.*1974C>G
ENST00000697683.1:c.*1677C>G	ENSP00000513395.1:n.*1677C>G
ENST00000697684.1:n.873C>G
ENST00000697685.1:c.*1510C>G	ENSP00000513396.1:n.*1510C>G
ENST00000697686.1:c.462C>G	ENSP00000513397.1:p.Ser154Arg
ENST00000697687.1:n.692C>G
ENST00000697688.1:n.859C>G
ENST00000697689.1:c.*1349C>G	ENSP00000513398.1:n.*1349C>G
ENST00000697690.1:c.813C>G	ENSP00000513399.1:p.Ser271Arg
ENST00000697691.1:c.*785C>G	ENSP00000513400.1:n.*785C>G
ENST00000697692.1:c.*825C>G	ENSP00000513401.1:n.*825C>G
ENST00000697694.1:c.462C>G	ENSP00000513402.1:p.Ser154Arg
ENST00000697695.1:n.1420C>G
ENST00000337432.9:c.813C>G MANE Select	ENSP00000336701.4:p.Ser271Arg
ENST00000337432.8:c.813C>G	ENSP00000336701.4:p.Ser271Arg
ENST00000413590.5:c.451C>G
ENST00000475762.5:c.*1516C>G	ENSP00000432421.1:n.*1516C>G
ENST00000482007.5:c.*241C>G	ENSP00000433332.1:n.*241C>G
ENST00000487525.5:c.*386C>G	ENSP00000431637.1:n.*386C>G
ENST00000578151.1:n.148C>G
ENST00000581221.5:n.328C>G
ENST00000583539.5:c.813C>G	ENSP00000463121.1:p.Ser271Arg
ENST00000584617.5:c.535C>G
ENST00000584804.1:c.108C>G	ENSP00000463658.1:p.Ser36Arg
NM_058216.2:c.813C>G	NP_478123.1:p.Ser271Arg
NR_103872.1:n.717C>G
XM_006722001.2:c.813C>G	XP_006722064.1:p.Ser271Arg
XM_006722002.2:c.813C>G	XP_006722065.1:p.Ser271Arg
XM_006722004.2:c.462C>G	XP_006722067.1:p.Ser154Arg
XM_006722005.2:c.462C>G	XP_006722068.1:p.Ser154Arg
XM_011525092.1:c.462C>G	XP_011523394.1:p.Ser154Arg
XM_011525093.1:c.462C>G	XP_011523395.1:p.Ser154Arg
XM_011525094.1:c.462C>G	XP_011523396.1:p.Ser154Arg
XR_934513.1:n.1031C>G
XR_934514.1:n.1031C>G
XM_006722001.4:c.813C>G	XP_006722064.1:p.Ser271Arg
XM_006722002.4:c.813C>G	XP_006722065.1:p.Ser271Arg
XM_006722004.3:c.462C>G	XP_006722067.1:p.Ser154Arg
XM_006722005.3:c.462C>G	XP_006722068.1:p.Ser154Arg
XM_011525092.2:c.462C>G	XP_011523394.1:p.Ser154Arg
XM_011525093.2:c.462C>G	XP_011523395.1:p.Ser154Arg
XM_011525094.2:c.462C>G	XP_011523396.1:p.Ser154Arg
XM_017024914.1:c.462C>G	XP_016880403.1:p.Ser154Arg
XM_017024915.1:c.462C>G	XP_016880404.1:p.Ser154Arg
XM_017024916.1:c.462C>G	XP_016880405.1:p.Ser154Arg
XM_017024917.1:c.462C>G	XP_016880406.1:p.Ser154Arg
XM_017024918.2:c.462C>G	XP_016880407.1:p.Ser154Arg
XM_017024919.1:c.462C>G	XP_016880408.1:p.Ser154Arg
XR_934513.3:n.1462C>G
XR_934514.3:n.1462C>G
NM_058216.3:c.813C>G MANE Select	NP_478123.1:p.Ser271Arg
NR_103872.2:n.688C>G