Canonical Allele Identifier: CA400349965

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56780664C>A (hg19) ; chr17:g.58703303C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58703303C>A , CM000679.2:g.58703303C>A	GRCh38
NC_000017.10:g.56780664C>A , CM000679.1:g.56780664C>A	GRCh37
NC_000017.9:g.54135663C>A	NCBI36
NG_023199.1:g.15702C>A , LRG_314:g.15702C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.328C>A	ENSP00000464056.2:p.Pro110Thr
ENST00000697677.1:n.1760C>A
ENST00000697678.1:n.581C>A
ENST00000697679.1:n.1753C>A
ENST00000697680.1:c.*1543C>A	ENSP00000513392.1:n.*1543C>A
ENST00000697681.1:c.*1695C>A	ENSP00000513393.1:n.*1695C>A
ENST00000697683.1:c.*1543C>A	ENSP00000513395.1:n.*1543C>A
ENST00000697684.1:n.739C>A
ENST00000697685.1:c.*1376C>A	ENSP00000513396.1:n.*1376C>A
ENST00000697686.1:c.328C>A	ENSP00000513397.1:p.Pro110Thr
ENST00000697687.1:n.558C>A
ENST00000697688.1:n.725C>A
ENST00000697689.1:c.*1215C>A	ENSP00000513398.1:n.*1215C>A
ENST00000697690.1:c.679C>A	ENSP00000513399.1:p.Pro227Thr
ENST00000697691.1:c.*651C>A	ENSP00000513400.1:n.*651C>A
ENST00000697692.1:c.*691C>A	ENSP00000513401.1:n.*691C>A
ENST00000697694.1:c.328C>A	ENSP00000513402.1:p.Pro110Thr
ENST00000697695.1:n.1286C>A
ENST00000337432.9:c.679C>A MANE Select	ENSP00000336701.4:p.Pro227Thr
ENST00000337432.8:c.679C>A	ENSP00000336701.4:p.Pro227Thr
ENST00000413590.5:c.317C>A
ENST00000425173.5:c.475C>A	ENSP00000407282.1:p.Pro159Thr
ENST00000461271.5:c.328C>A	ENSP00000464056.1:p.Pro110Thr
ENST00000475762.5:c.*1382C>A	ENSP00000432421.1:n.*1382C>A
ENST00000482007.5:c.*107C>A	ENSP00000433332.1:n.*107C>A
ENST00000487525.5:c.*107C>A	ENSP00000431637.1:n.*107C>A
ENST00000487921.5:n.591C>A
ENST00000583539.5:c.679C>A	ENSP00000463121.1:p.Pro227Thr
ENST00000584617.5:c.401C>A
NM_058216.2:c.679C>A	NP_478123.1:p.Pro227Thr
NR_103872.1:n.583C>A
XM_006722001.2:c.679C>A	XP_006722064.1:p.Pro227Thr
XM_006722002.2:c.679C>A	XP_006722065.1:p.Pro227Thr
XM_006722004.2:c.328C>A	XP_006722067.1:p.Pro110Thr
XM_006722005.2:c.328C>A	XP_006722068.1:p.Pro110Thr
XM_011525092.1:c.328C>A	XP_011523394.1:p.Pro110Thr
XM_011525093.1:c.328C>A	XP_011523395.1:p.Pro110Thr
XM_011525094.1:c.328C>A	XP_011523396.1:p.Pro110Thr
XR_934513.1:n.752C>A
XR_934514.1:n.752C>A
XM_006722001.4:c.679C>A	XP_006722064.1:p.Pro227Thr
XM_006722002.4:c.679C>A	XP_006722065.1:p.Pro227Thr
XM_006722004.3:c.328C>A	XP_006722067.1:p.Pro110Thr
XM_006722005.3:c.328C>A	XP_006722068.1:p.Pro110Thr
XM_011525092.2:c.328C>A	XP_011523394.1:p.Pro110Thr
XM_011525093.2:c.328C>A	XP_011523395.1:p.Pro110Thr
XM_011525094.2:c.328C>A	XP_011523396.1:p.Pro110Thr
XM_017024914.1:c.328C>A	XP_016880403.1:p.Pro110Thr
XM_017024915.1:c.328C>A	XP_016880404.1:p.Pro110Thr
XM_017024916.1:c.328C>A	XP_016880405.1:p.Pro110Thr
XM_017024917.1:c.328C>A	XP_016880406.1:p.Pro110Thr
XM_017024918.2:c.328C>A	XP_016880407.1:p.Pro110Thr
XM_017024919.1:c.328C>A	XP_016880408.1:p.Pro110Thr
XR_934513.3:n.1183C>A
XR_934514.3:n.1183C>A
NM_058216.3:c.679C>A MANE Select	NP_478123.1:p.Pro227Thr
NR_103872.2:n.554C>A