Canonical Allele Identifier: CA400361305

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 584558
• ClinVar RCV Id: RCV000708747 ; RCV000989965
• dbSNP Id: rs876659009
• MyVariant Identifiers: chr17:g.56801408T>G (hg19) ; chr17:g.58724047T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724047T>G , CM000679.2:g.58724047T>G	GRCh38
NC_000017.10:g.56801408T>G , CM000679.1:g.56801408T>G	GRCh37
NC_000017.9:g.54156407T>G	NCBI36
NG_023199.1:g.36446T>G , LRG_314:g.36446T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.561T>G	ENSP00000464056.2:p.Ser187Arg
ENST00000697680.1:c.*1876T>G	ENSP00000513392.1:n.*1876T>G
ENST00000697681.1:c.*2073T>G	ENSP00000513393.1:n.*2073T>G
ENST00000697683.1:c.*1776T>G	ENSP00000513395.1:n.*1776T>G
ENST00000697684.1:n.972T>G
ENST00000697685.1:c.*1609T>G	ENSP00000513396.1:n.*1609T>G
ENST00000697686.1:c.561T>G	ENSP00000513397.1:p.Ser187Arg
ENST00000697687.1:n.791T>G
ENST00000697688.1:n.958T>G
ENST00000697689.1:c.*1440+3235T>G	ENSP00000513398.1:n.*1440+3235T>G
ENST00000697690.1:c.904+3235T>G	ENSP00000513399.1:n.904+3235T>G
ENST00000697691.1:c.*884T>G	ENSP00000513400.1:n.*884T>G
ENST00000697692.1:c.*924T>G	ENSP00000513401.1:n.*924T>G
ENST00000697694.1:c.561T>G	ENSP00000513402.1:p.Ser187Arg
ENST00000697695.1:n.1519T>G
ENST00000337432.9:c.912T>G MANE Select	ENSP00000336701.4:p.Ser304Arg
ENST00000337432.8:c.912T>G	ENSP00000336701.4:p.Ser304Arg
ENST00000413590.5:c.550T>G
ENST00000475762.5:c.*1548T>G	ENSP00000432421.1:n.*1548T>G
ENST00000482007.5:c.*340T>G	ENSP00000433332.1:n.*340T>G
ENST00000487525.5:c.*485T>G	ENSP00000431637.1:n.*485T>G
ENST00000578151.1:n.239+3235T>G
ENST00000581221.5:n.427T>G
ENST00000583539.5:c.912T>G	ENSP00000463121.1:p.Ser304Arg
ENST00000584617.5:c.634T>G
ENST00000584804.1:c.199+3235T>G	ENSP00000463658.1:n.199+3235T>G
NM_058216.2:c.912T>G	NP_478123.1:p.Ser304Arg
NR_103872.1:n.816T>G
XM_006722001.2:c.912T>G	XP_006722064.1:p.Ser304Arg
XM_006722002.2:c.904+3235T>G	XP_006722065.1:n.904+3235T>G
XM_006722004.2:c.561T>G	XP_006722067.1:p.Ser187Arg
XM_006722005.2:c.561T>G	XP_006722068.1:p.Ser187Arg
XM_011525092.1:c.561T>G	XP_011523394.1:p.Ser187Arg
XM_011525093.1:c.561T>G	XP_011523395.1:p.Ser187Arg
XM_011525094.1:c.561T>G	XP_011523396.1:p.Ser187Arg
XR_934513.1:n.1130T>G
XR_934514.1:n.1130T>G
XM_006722001.4:c.912T>G	XP_006722064.1:p.Ser304Arg
XM_006722002.4:c.904+3235T>G	XP_006722065.1:n.904+3235T>G
XM_006722004.3:c.561T>G	XP_006722067.1:p.Ser187Arg
XM_006722005.3:c.561T>G	XP_006722068.1:p.Ser187Arg
XM_011525092.2:c.561T>G	XP_011523394.1:p.Ser187Arg
XM_011525093.2:c.561T>G	XP_011523395.1:p.Ser187Arg
XM_011525094.2:c.561T>G	XP_011523396.1:p.Ser187Arg
XM_017024914.1:c.561T>G	XP_016880403.1:p.Ser187Arg
XM_017024915.1:c.561T>G	XP_016880404.1:p.Ser187Arg
XM_017024916.1:c.561T>G	XP_016880405.1:p.Ser187Arg
XM_017024917.1:c.561T>G	XP_016880406.1:p.Ser187Arg
XM_017024918.2:c.561T>G	XP_016880407.1:p.Ser187Arg
XM_017024919.1:c.553+3235T>G	XP_016880408.1:n.553+3235T>G
XR_934513.3:n.1561T>G
XR_934514.3:n.1561T>G
NM_058216.3:c.912T>G MANE Select	NP_478123.1:p.Ser304Arg
NR_103872.2:n.787T>G