Canonical Allele Identifier: CA10583607

Gene: RAD51C

Linked Data

• ClinVar Variation Id: 241779
• ClinVar RCV Id: RCV000226369 ; RCV000409098 ; RCV000481912 ; RCV003317171 ; RCV003298308
• dbSNP Id: rs760235677
• MyVariant Identifiers: chr17:g.56787352G>T (hg19) ; chr17:g.58709991G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709991G>T , CM000679.2:g.58709991G>T	GRCh38
NC_000017.10:g.56787352G>T , CM000679.1:g.56787352G>T	GRCh37
NC_000017.9:g.54142351G>T	NCBI36
NG_023199.1:g.22390G>T , LRG_314:g.22390G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.486+1G>T	ENSP00000464056.2:n.486+1G>T
ENST00000697678.1:n.739+1G>T
ENST00000697679.1:n.1911+1G>T
ENST00000697680.1:c.*1701+1G>T	ENSP00000513392.1:n.*1701+1G>T
ENST00000697681.1:c.*1998+1G>T	ENSP00000513393.1:n.*1998+1G>T
ENST00000697683.1:c.*1701+1G>T	ENSP00000513395.1:n.*1701+1G>T
ENST00000697684.1:n.897+1G>T
ENST00000697685.1:c.*1534+1G>T	ENSP00000513396.1:n.*1534+1G>T
ENST00000697686.1:c.486+1G>T	ENSP00000513397.1:n.486+1G>T
ENST00000697687.1:n.716+1G>T
ENST00000697688.1:n.883+1G>T
ENST00000697689.1:c.*1373+1G>T	ENSP00000513398.1:n.*1373+1G>T
ENST00000697690.1:c.837+1G>T	ENSP00000513399.1:n.837+1G>T
ENST00000697691.1:c.*809+1G>T	ENSP00000513400.1:n.*809+1G>T
ENST00000697692.1:c.*849+1G>T	ENSP00000513401.1:n.*849+1G>T
ENST00000697694.1:c.486+1G>T	ENSP00000513402.1:n.486+1G>T
ENST00000697695.1:n.1444+1G>T
ENST00000337432.9:c.837+1G>T MANE Select	ENSP00000336701.4:n.837+1G>T
ENST00000337432.8:c.837+1G>T	ENSP00000336701.4:n.837+1G>T
ENST00000413590.5:c.475+1G>T
ENST00000475762.5:c.*1540+1G>T	ENSP00000432421.1:n.*1540+1G>T
ENST00000482007.5:c.*265+1G>T	ENSP00000433332.1:n.*265+1G>T
ENST00000487525.5:c.*410+1G>T	ENSP00000431637.1:n.*410+1G>T
ENST00000578151.1:n.172+1G>T
ENST00000581221.5:n.352+1G>T
ENST00000583539.5:c.837+1G>T	ENSP00000463121.1:n.837+1G>T
ENST00000584617.5:c.559+1G>T
ENST00000584804.1:c.132+1G>T	ENSP00000463658.1:n.132+1G>T
NM_058216.2:c.837+1G>T	NP_478123.1:n.837+1G>T
NR_103872.1:n.741+1G>T
XM_006722001.2:c.837+1G>T	XP_006722064.1:n.837+1G>T
XM_006722002.2:c.837+1G>T	XP_006722065.1:n.837+1G>T
XM_006722004.2:c.486+1G>T	XP_006722067.1:n.486+1G>T
XM_006722005.2:c.486+1G>T	XP_006722068.1:n.486+1G>T
XM_011525092.1:c.486+1G>T	XP_011523394.1:n.486+1G>T
XM_011525093.1:c.486+1G>T	XP_011523395.1:n.486+1G>T
XM_011525094.1:c.486+1G>T	XP_011523396.1:n.486+1G>T
XR_934513.1:n.1055+1G>T
XR_934514.1:n.1055+1G>T
XM_006722001.4:c.837+1G>T	XP_006722064.1:n.837+1G>T
XM_006722002.4:c.837+1G>T	XP_006722065.1:n.837+1G>T
XM_006722004.3:c.486+1G>T	XP_006722067.1:n.486+1G>T
XM_006722005.3:c.486+1G>T	XP_006722068.1:n.486+1G>T
XM_011525092.2:c.486+1G>T	XP_011523394.1:n.486+1G>T
XM_011525093.2:c.486+1G>T	XP_011523395.1:n.486+1G>T
XM_011525094.2:c.486+1G>T	XP_011523396.1:n.486+1G>T
XM_017024914.1:c.486+1G>T	XP_016880403.1:n.486+1G>T
XM_017024915.1:c.486+1G>T	XP_016880404.1:n.486+1G>T
XM_017024916.1:c.486+1G>T	XP_016880405.1:n.486+1G>T
XM_017024917.1:c.486+1G>T	XP_016880406.1:n.486+1G>T
XM_017024918.2:c.486+1G>T	XP_016880407.1:n.486+1G>T
XM_017024919.1:c.486+1G>T	XP_016880408.1:n.486+1G>T
XR_934513.3:n.1486+1G>T
XR_934514.3:n.1486+1G>T
NM_058216.3:c.837+1G>T MANE Select	NP_478123.1:n.837+1G>T
NR_103872.2:n.712+1G>T