Canonical Allele Identifier: CA400365296

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 2024574
• ClinVar RCV Id: RCV002847791
• MyVariant Identifiers: chr17:g.56809909A>T (hg19) ; chr17:g.58732548A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58732548A>T , CM000679.2:g.58732548A>T	GRCh38
NC_000017.10:g.56809909A>T , CM000679.1:g.56809909A>T	GRCh37
NC_000017.9:g.54164908A>T	NCBI36
NG_023199.1:g.44947A>T , LRG_314:g.44947A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.679A>T	ENSP00000464056.2:p.Ser227Cys
ENST00000697680.1:c.*1990+4A>T	ENSP00000513392.1:n.*1990+4A>T
ENST00000697681.1:c.*2187+4A>T	ENSP00000513393.1:n.*2187+4A>T
ENST00000697683.1:c.*1962+4A>T	ENSP00000513395.1:n.*1962+4A>T
ENST00000697685.1:c.*1723+4A>T	ENSP00000513396.1:n.*1723+4A>T
ENST00000697686.1:c.797+4A>T	ENSP00000513397.1:n.797+4A>T
ENST00000697689.1:c.*1441-1570A>T	ENSP00000513398.1:n.*1441-1570A>T
ENST00000697690.1:c.905-1570A>T	ENSP00000513399.1:n.905-1570A>T
ENST00000697691.1:c.*998+4A>T	ENSP00000513400.1:n.*998+4A>T
ENST00000697692.1:c.*1038+4A>T	ENSP00000513401.1:n.*1038+4A>T
ENST00000697694.1:c.675+4A>T	ENSP00000513402.1:n.675+4A>T
ENST00000697695.1:n.1633+4A>T
ENST00000337432.9:c.1026+4A>T MANE Select	ENSP00000336701.4:n.1026+4A>T
ENST00000337432.8:c.1026+4A>T	ENSP00000336701.4:n.1026+4A>T
ENST00000413590.5:c.667+4A>T
ENST00000461706.1:n.213+4A>T
ENST00000475762.5:c.*1662+4A>T	ENSP00000432421.1:n.*1662+4A>T
ENST00000482007.5:c.*454+4A>T	ENSP00000433332.1:n.*454+4A>T
ENST00000487525.5:c.*602+4A>T	ENSP00000431637.1:n.*602+4A>T
ENST00000578151.1:n.240-1570A>T
ENST00000581221.5:n.541+4A>T
ENST00000583539.5:c.1030A>T	ENSP00000463121.1:p.Ser344Cys
ENST00000584804.1:c.260+4A>T	ENSP00000463658.1:n.260+4A>T
NM_058216.2:c.1026+4A>T	NP_478123.1:n.1026+4A>T
NR_103872.1:n.930+4A>T
XM_006722001.2:c.1029+4A>T	XP_006722064.1:n.1029+4A>T
XM_006722002.2:c.965+4A>T	XP_006722065.1:n.965+4A>T
XM_006722004.2:c.678+4A>T	XP_006722067.1:n.678+4A>T
XM_006722005.2:c.678+4A>T	XP_006722068.1:n.678+4A>T
XM_011525092.1:c.678+4A>T	XP_011523394.1:n.678+4A>T
XM_011525093.1:c.678+4A>T	XP_011523395.1:n.678+4A>T
XM_011525094.1:c.678+4A>T	XP_011523396.1:n.678+4A>T
XR_934513.1:n.1244+4A>T
XR_934514.1:n.1247+4A>T
XR_934886.1:n.149+5523T>A
XM_006722001.4:c.1029+4A>T	XP_006722064.1:n.1029+4A>T
XM_006722002.4:c.965+4A>T	XP_006722065.1:n.965+4A>T
XM_006722004.3:c.678+4A>T	XP_006722067.1:n.678+4A>T
XM_006722005.3:c.678+4A>T	XP_006722068.1:n.678+4A>T
XM_011525092.2:c.678+4A>T	XP_011523394.1:n.678+4A>T
XM_011525093.2:c.678+4A>T	XP_011523395.1:n.678+4A>T
XM_011525094.2:c.678+4A>T	XP_011523396.1:n.678+4A>T
XM_017024914.1:c.675+4A>T	XP_016880403.1:n.675+4A>T
XM_017024915.1:c.675+4A>T	XP_016880404.1:n.675+4A>T
XM_017024916.1:c.675+4A>T	XP_016880405.1:n.675+4A>T
XM_017024917.1:c.675+4A>T	XP_016880406.1:n.675+4A>T
XM_017024918.2:c.675+4A>T	XP_016880407.1:n.675+4A>T
XM_017024919.1:c.614+4A>T	XP_016880408.1:n.614+4A>T
XR_934513.3:n.1675+4A>T
XR_934514.3:n.1678+4A>T
XR_934886.2:n.149+5523T>A
NM_058216.3:c.1026+4A>T MANE Select	NP_478123.1:n.1026+4A>T
NR_103872.2:n.901+4A>T