Canonical Allele Identifier: CA400361278

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 1209850
• ClinVar RCV Id: RCV001579300 ; RCV001866089
• dbSNP Id: rs2143961266
• MyVariant Identifiers: chr17:g.56801403G>T (hg19) ; chr17:g.58724042G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58724042G>T , CM000679.2:g.58724042G>T	GRCh38
NC_000017.10:g.56801403G>T , CM000679.1:g.56801403G>T	GRCh37
NC_000017.9:g.54156402G>T	NCBI36
NG_023199.1:g.36441G>T , LRG_314:g.36441G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.556G>T	ENSP00000464056.2:p.Glu186Ter
ENST00000697680.1:c.*1871G>T	ENSP00000513392.1:n.*1871G>T
ENST00000697681.1:c.*2068G>T	ENSP00000513393.1:n.*2068G>T
ENST00000697683.1:c.*1771G>T	ENSP00000513395.1:n.*1771G>T
ENST00000697684.1:n.967G>T
ENST00000697685.1:c.*1604G>T	ENSP00000513396.1:n.*1604G>T
ENST00000697686.1:c.556G>T	ENSP00000513397.1:p.Glu186Ter
ENST00000697687.1:n.786G>T
ENST00000697688.1:n.953G>T
ENST00000697689.1:c.*1440+3230G>T	ENSP00000513398.1:n.*1440+3230G>T
ENST00000697690.1:c.904+3230G>T	ENSP00000513399.1:n.904+3230G>T
ENST00000697691.1:c.*879G>T	ENSP00000513400.1:n.*879G>T
ENST00000697692.1:c.*919G>T	ENSP00000513401.1:n.*919G>T
ENST00000697694.1:c.556G>T	ENSP00000513402.1:p.Glu186Ter
ENST00000697695.1:n.1514G>T
ENST00000337432.9:c.907G>T MANE Select	ENSP00000336701.4:p.Glu303Ter
ENST00000337432.8:c.907G>T	ENSP00000336701.4:p.Glu303Ter
ENST00000413590.5:c.545G>T
ENST00000475762.5:c.*1543G>T	ENSP00000432421.1:n.*1543G>T
ENST00000482007.5:c.*335G>T	ENSP00000433332.1:n.*335G>T
ENST00000487525.5:c.*480G>T	ENSP00000431637.1:n.*480G>T
ENST00000578151.1:n.239+3230G>T
ENST00000581221.5:n.422G>T
ENST00000583539.5:c.907G>T	ENSP00000463121.1:p.Glu303Ter
ENST00000584617.5:c.629G>T
ENST00000584804.1:c.199+3230G>T	ENSP00000463658.1:n.199+3230G>T
NM_058216.2:c.907G>T	NP_478123.1:p.Glu303Ter
NR_103872.1:n.811G>T
XM_006722001.2:c.907G>T	XP_006722064.1:p.Glu303Ter
XM_006722002.2:c.904+3230G>T	XP_006722065.1:n.904+3230G>T
XM_006722004.2:c.556G>T	XP_006722067.1:p.Glu186Ter
XM_006722005.2:c.556G>T	XP_006722068.1:p.Glu186Ter
XM_011525092.1:c.556G>T	XP_011523394.1:p.Glu186Ter
XM_011525093.1:c.556G>T	XP_011523395.1:p.Glu186Ter
XM_011525094.1:c.556G>T	XP_011523396.1:p.Glu186Ter
XR_934513.1:n.1125G>T
XR_934514.1:n.1125G>T
XM_006722001.4:c.907G>T	XP_006722064.1:p.Glu303Ter
XM_006722002.4:c.904+3230G>T	XP_006722065.1:n.904+3230G>T
XM_006722004.3:c.556G>T	XP_006722067.1:p.Glu186Ter
XM_006722005.3:c.556G>T	XP_006722068.1:p.Glu186Ter
XM_011525092.2:c.556G>T	XP_011523394.1:p.Glu186Ter
XM_011525093.2:c.556G>T	XP_011523395.1:p.Glu186Ter
XM_011525094.2:c.556G>T	XP_011523396.1:p.Glu186Ter
XM_017024914.1:c.556G>T	XP_016880403.1:p.Glu186Ter
XM_017024915.1:c.556G>T	XP_016880404.1:p.Glu186Ter
XM_017024916.1:c.556G>T	XP_016880405.1:p.Glu186Ter
XM_017024917.1:c.556G>T	XP_016880406.1:p.Glu186Ter
XM_017024918.2:c.556G>T	XP_016880407.1:p.Glu186Ter
XM_017024919.1:c.553+3230G>T	XP_016880408.1:n.553+3230G>T
XR_934513.3:n.1556G>T
XR_934514.3:n.1556G>T
NM_058216.3:c.907G>T MANE Select	NP_478123.1:p.Glu303Ter
NR_103872.2:n.782G>T