Canonical Allele Identifier: CA400353594

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56787266A>C (hg19) ; chr17:g.58709905A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709905A>C , CM000679.2:g.58709905A>C	GRCh38
NC_000017.10:g.56787266A>C , CM000679.1:g.56787266A>C	GRCh37
NC_000017.9:g.54142265A>C	NCBI36
NG_023199.1:g.22304A>C , LRG_314:g.22304A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.401A>C	ENSP00000464056.2:p.Asp134Ala
ENST00000697678.1:n.654A>C
ENST00000697679.1:n.1826A>C
ENST00000697680.1:c.*1616A>C	ENSP00000513392.1:n.*1616A>C
ENST00000697681.1:c.*1913A>C	ENSP00000513393.1:n.*1913A>C
ENST00000697683.1:c.*1616A>C	ENSP00000513395.1:n.*1616A>C
ENST00000697684.1:n.812A>C
ENST00000697685.1:c.*1449A>C	ENSP00000513396.1:n.*1449A>C
ENST00000697686.1:c.401A>C	ENSP00000513397.1:p.Asp134Ala
ENST00000697687.1:n.631A>C
ENST00000697688.1:n.798A>C
ENST00000697689.1:c.*1288A>C	ENSP00000513398.1:n.*1288A>C
ENST00000697690.1:c.752A>C	ENSP00000513399.1:p.Asp251Ala
ENST00000697691.1:c.*724A>C	ENSP00000513400.1:n.*724A>C
ENST00000697692.1:c.*764A>C	ENSP00000513401.1:n.*764A>C
ENST00000697694.1:c.401A>C	ENSP00000513402.1:p.Asp134Ala
ENST00000697695.1:n.1359A>C
ENST00000337432.9:c.752A>C MANE Select	ENSP00000336701.4:p.Asp251Ala
ENST00000337432.8:c.752A>C	ENSP00000336701.4:p.Asp251Ala
ENST00000413590.5:c.390A>C
ENST00000461271.5:c.401A>C	ENSP00000464056.1:p.Asp134Ala
ENST00000475762.5:c.*1455A>C	ENSP00000432421.1:n.*1455A>C
ENST00000482007.5:c.*180A>C	ENSP00000433332.1:n.*180A>C
ENST00000487525.5:c.*325A>C	ENSP00000431637.1:n.*325A>C
ENST00000578151.1:n.87A>C
ENST00000581221.5:n.267A>C
ENST00000583539.5:c.752A>C	ENSP00000463121.1:p.Asp251Ala
ENST00000584617.5:c.474A>C
ENST00000584804.1:c.47A>C	ENSP00000463658.1:p.Asp16Ala
NM_058216.2:c.752A>C	NP_478123.1:p.Asp251Ala
NR_103872.1:n.656A>C
XM_006722001.2:c.752A>C	XP_006722064.1:p.Asp251Ala
XM_006722002.2:c.752A>C	XP_006722065.1:p.Asp251Ala
XM_006722004.2:c.401A>C	XP_006722067.1:p.Asp134Ala
XM_006722005.2:c.401A>C	XP_006722068.1:p.Asp134Ala
XM_011525092.1:c.401A>C	XP_011523394.1:p.Asp134Ala
XM_011525093.1:c.401A>C	XP_011523395.1:p.Asp134Ala
XM_011525094.1:c.401A>C	XP_011523396.1:p.Asp134Ala
XR_934513.1:n.970A>C
XR_934514.1:n.970A>C
XM_006722001.4:c.752A>C	XP_006722064.1:p.Asp251Ala
XM_006722002.4:c.752A>C	XP_006722065.1:p.Asp251Ala
XM_006722004.3:c.401A>C	XP_006722067.1:p.Asp134Ala
XM_006722005.3:c.401A>C	XP_006722068.1:p.Asp134Ala
XM_011525092.2:c.401A>C	XP_011523394.1:p.Asp134Ala
XM_011525093.2:c.401A>C	XP_011523395.1:p.Asp134Ala
XM_011525094.2:c.401A>C	XP_011523396.1:p.Asp134Ala
XM_017024914.1:c.401A>C	XP_016880403.1:p.Asp134Ala
XM_017024915.1:c.401A>C	XP_016880404.1:p.Asp134Ala
XM_017024916.1:c.401A>C	XP_016880405.1:p.Asp134Ala
XM_017024917.1:c.401A>C	XP_016880406.1:p.Asp134Ala
XM_017024918.2:c.401A>C	XP_016880407.1:p.Asp134Ala
XM_017024919.1:c.401A>C	XP_016880408.1:p.Asp134Ala
XR_934513.3:n.1401A>C
XR_934514.3:n.1401A>C
NM_058216.3:c.752A>C MANE Select	NP_478123.1:p.Asp251Ala
NR_103872.2:n.627A>C