Canonical Allele Identifier: CA400353536

Gene: RAD51C

Linked Data

• dbSNP Id: rs730881925
• MyVariant Identifiers: chr17:g.56787260G>T (hg19) ; chr17:g.58709899G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709899G>T , CM000679.2:g.58709899G>T	GRCh38
NC_000017.10:g.56787260G>T , CM000679.1:g.56787260G>T	GRCh37
NC_000017.9:g.54142259G>T	NCBI36
NG_023199.1:g.22298G>T , LRG_314:g.22298G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.395G>T	ENSP00000464056.2:p.Arg132Leu
ENST00000697678.1:n.648G>T
ENST00000697679.1:n.1820G>T
ENST00000697680.1:c.*1610G>T	ENSP00000513392.1:n.*1610G>T
ENST00000697681.1:c.*1907G>T	ENSP00000513393.1:n.*1907G>T
ENST00000697683.1:c.*1610G>T	ENSP00000513395.1:n.*1610G>T
ENST00000697684.1:n.806G>T
ENST00000697685.1:c.*1443G>T	ENSP00000513396.1:n.*1443G>T
ENST00000697686.1:c.395G>T	ENSP00000513397.1:p.Arg132Leu
ENST00000697687.1:n.625G>T
ENST00000697688.1:n.792G>T
ENST00000697689.1:c.*1282G>T	ENSP00000513398.1:n.*1282G>T
ENST00000697690.1:c.746G>T	ENSP00000513399.1:p.Arg249Leu
ENST00000697691.1:c.*718G>T	ENSP00000513400.1:n.*718G>T
ENST00000697692.1:c.*758G>T	ENSP00000513401.1:n.*758G>T
ENST00000697694.1:c.395G>T	ENSP00000513402.1:p.Arg132Leu
ENST00000697695.1:n.1353G>T
ENST00000337432.9:c.746G>T MANE Select	ENSP00000336701.4:p.Arg249Leu
ENST00000337432.8:c.746G>T	ENSP00000336701.4:p.Arg249Leu
ENST00000413590.5:c.384G>T
ENST00000461271.5:c.395G>T	ENSP00000464056.1:p.Arg132Leu
ENST00000475762.5:c.*1449G>T	ENSP00000432421.1:n.*1449G>T
ENST00000482007.5:c.*174G>T	ENSP00000433332.1:n.*174G>T
ENST00000487525.5:c.*319G>T	ENSP00000431637.1:n.*319G>T
ENST00000578151.1:n.81G>T
ENST00000581221.5:n.261G>T
ENST00000583539.5:c.746G>T	ENSP00000463121.1:p.Arg249Leu
ENST00000584617.5:c.468G>T
ENST00000584804.1:c.41G>T	ENSP00000463658.1:p.Arg14Leu
NM_058216.2:c.746G>T	NP_478123.1:p.Arg249Leu
NR_103872.1:n.650G>T
XM_006722001.2:c.746G>T	XP_006722064.1:p.Arg249Leu
XM_006722002.2:c.746G>T	XP_006722065.1:p.Arg249Leu
XM_006722004.2:c.395G>T	XP_006722067.1:p.Arg132Leu
XM_006722005.2:c.395G>T	XP_006722068.1:p.Arg132Leu
XM_011525092.1:c.395G>T	XP_011523394.1:p.Arg132Leu
XM_011525093.1:c.395G>T	XP_011523395.1:p.Arg132Leu
XM_011525094.1:c.395G>T	XP_011523396.1:p.Arg132Leu
XR_934513.1:n.964G>T
XR_934514.1:n.964G>T
XM_006722001.4:c.746G>T	XP_006722064.1:p.Arg249Leu
XM_006722002.4:c.746G>T	XP_006722065.1:p.Arg249Leu
XM_006722004.3:c.395G>T	XP_006722067.1:p.Arg132Leu
XM_006722005.3:c.395G>T	XP_006722068.1:p.Arg132Leu
XM_011525092.2:c.395G>T	XP_011523394.1:p.Arg132Leu
XM_011525093.2:c.395G>T	XP_011523395.1:p.Arg132Leu
XM_011525094.2:c.395G>T	XP_011523396.1:p.Arg132Leu
XM_017024914.1:c.395G>T	XP_016880403.1:p.Arg132Leu
XM_017024915.1:c.395G>T	XP_016880404.1:p.Arg132Leu
XM_017024916.1:c.395G>T	XP_016880405.1:p.Arg132Leu
XM_017024917.1:c.395G>T	XP_016880406.1:p.Arg132Leu
XM_017024918.2:c.395G>T	XP_016880407.1:p.Arg132Leu
XM_017024919.1:c.395G>T	XP_016880408.1:p.Arg132Leu
XR_934513.3:n.1395G>T
XR_934514.3:n.1395G>T
NM_058216.3:c.746G>T MANE Select	NP_478123.1:p.Arg249Leu
NR_103872.2:n.621G>T