Canonical Allele Identifier: CA400339978

Gene: RAD51C

Linked Data

• dbSNP Id: rs375451955
• MyVariant Identifiers: chr17:g.56772346A>T (hg19) ; chr17:g.58694985A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694985A>T , CM000679.2:g.58694985A>T	GRCh38
NC_000017.10:g.56772346A>T , CM000679.1:g.56772346A>T	GRCh37
NC_000017.9:g.54127345A>T	NCBI36
NG_023199.1:g.7384A>T , LRG_314:g.7384A>T
NG_047169.1:g.2095T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-152A>T	ENSP00000464056.2:n.-152A>T
ENST00000697675.1:n.1294A>T
ENST00000697676.1:n.260A>T
ENST00000697677.1:n.1281A>T
ENST00000697678.1:n.102A>T
ENST00000697679.1:n.1274A>T
ENST00000697680.1:c.*1064A>T	ENSP00000513392.1:n.*1064A>T
ENST00000697681.1:c.*1064A>T	ENSP00000513393.1:n.*1064A>T
ENST00000697683.1:c.*1064A>T	ENSP00000513395.1:n.*1064A>T
ENST00000697684.1:n.260A>T
ENST00000697685.1:c.*1064A>T	ENSP00000513396.1:n.*1064A>T
ENST00000697686.1:c.-152A>T	ENSP00000513397.1:n.-152A>T
ENST00000697687.1:n.246A>T
ENST00000697688.1:n.246A>T
ENST00000697689.1:c.*903A>T	ENSP00000513398.1:n.*903A>T
ENST00000697690.1:c.200A>T	ENSP00000513399.1:p.Glu67Val
ENST00000697691.1:c.*172A>T	ENSP00000513400.1:n.*172A>T
ENST00000697692.1:c.*212A>T	ENSP00000513401.1:n.*212A>T
ENST00000697693.1:n.975A>T
ENST00000697694.1:c.-152A>T	ENSP00000513402.1:n.-152A>T
ENST00000697695.1:n.807A>T
ENST00000337432.9:c.200A>T MANE Select	ENSP00000336701.4:p.Glu67Val
ENST00000337432.8:c.200A>T	ENSP00000336701.4:p.Glu67Val
ENST00000421782.3:c.200A>T	ENSP00000391450.2:p.Glu67Val
ENST00000461271.5:c.-152A>T	ENSP00000464056.1:n.-152A>T
ENST00000475762.5:c.*903A>T	ENSP00000432421.1:n.*903A>T
ENST00000482007.5:c.200A>T	ENSP00000433332.1:p.Glu67Val
ENST00000486827.1:c.*1064A>T	ENSP00000436761.1:n.*1064A>T
ENST00000487525.5:c.200A>T	ENSP00000431637.1:p.Glu67Val
ENST00000487921.5:n.112A>T
ENST00000583539.5:c.200A>T	ENSP00000463121.1:p.Glu67Val
ENST00000584617.5:c.127-1708A>T
NM_002876.3:c.200A>T	NP_002867.1:p.Glu67Val
NM_058216.2:c.200A>T	NP_478123.1:p.Glu67Val
NR_103872.1:n.271A>T
NR_103873.1:n.168A>T
XM_006722001.2:c.200A>T	XP_006722064.1:p.Glu67Val
XM_006722002.2:c.200A>T	XP_006722065.1:p.Glu67Val
XM_006722004.2:c.-152A>T	XP_006722067.1:n.-152A>T
XM_006722005.2:c.-152A>T	XP_006722068.1:n.-152A>T
XM_011525092.1:c.-152A>T	XP_011523394.1:n.-152A>T
XM_011525093.1:c.-152A>T	XP_011523395.1:n.-152A>T
XM_011525094.1:c.-152A>T	XP_011523396.1:n.-152A>T
XR_934513.1:n.273A>T
XR_934514.1:n.273A>T
XM_006722001.4:c.200A>T	XP_006722064.1:p.Glu67Val
XM_006722002.4:c.200A>T	XP_006722065.1:p.Glu67Val
XM_006722004.3:c.-152A>T	XP_006722067.1:n.-152A>T
XM_006722005.3:c.-152A>T	XP_006722068.1:n.-152A>T
XM_011525092.2:c.-152A>T	XP_011523394.1:n.-152A>T
XM_011525093.2:c.-152A>T	XP_011523395.1:n.-152A>T
XM_011525094.2:c.-152A>T	XP_011523396.1:n.-152A>T
XM_017024914.1:c.-152A>T	XP_016880403.1:n.-152A>T
XM_017024915.1:c.-152A>T	XP_016880404.1:n.-152A>T
XM_017024916.1:c.-152A>T	XP_016880405.1:n.-152A>T
XM_017024917.1:c.-152A>T	XP_016880406.1:n.-152A>T
XM_017024918.2:c.-152A>T	XP_016880407.1:n.-152A>T
XM_017024919.1:c.-152A>T	XP_016880408.1:n.-152A>T
XR_934513.3:n.704A>T
XR_934514.3:n.704A>T
NM_058216.3:c.200A>T MANE Select	NP_478123.1:p.Glu67Val
NR_103872.2:n.242A>T
NM_002876.4:c.200A>T	NP_002867.1:p.Glu67Val