Canonical Allele Identifier: CA400339771

Gene: RAD51C

Linked Data

• dbSNP Id: rs2143718529
• MyVariant Identifiers: chr17:g.56772327C>G (hg19) ; chr17:g.58694966C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58694966C>G , CM000679.2:g.58694966C>G	GRCh38
NC_000017.10:g.56772327C>G , CM000679.1:g.56772327C>G	GRCh37
NC_000017.9:g.54127326C>G	NCBI36
NG_023199.1:g.7365C>G , LRG_314:g.7365C>G
NG_047169.1:g.2114G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000461271.6:c.-171C>G	ENSP00000464056.2:n.-171C>G
ENST00000697675.1:n.1275C>G
ENST00000697676.1:n.241C>G
ENST00000697677.1:n.1262C>G
ENST00000697678.1:n.83C>G
ENST00000697679.1:n.1255C>G
ENST00000697680.1:c.*1045C>G	ENSP00000513392.1:n.*1045C>G
ENST00000697681.1:c.*1045C>G	ENSP00000513393.1:n.*1045C>G
ENST00000697683.1:c.*1045C>G	ENSP00000513395.1:n.*1045C>G
ENST00000697684.1:n.241C>G
ENST00000697685.1:c.*1045C>G	ENSP00000513396.1:n.*1045C>G
ENST00000697686.1:c.-171C>G	ENSP00000513397.1:n.-171C>G
ENST00000697687.1:n.227C>G
ENST00000697688.1:n.227C>G
ENST00000697689.1:c.*884C>G	ENSP00000513398.1:n.*884C>G
ENST00000697690.1:c.181C>G	ENSP00000513399.1:p.Leu61Val
ENST00000697691.1:c.*153C>G	ENSP00000513400.1:n.*153C>G
ENST00000697692.1:c.*193C>G	ENSP00000513401.1:n.*193C>G
ENST00000697693.1:n.956C>G
ENST00000697694.1:c.-171C>G	ENSP00000513402.1:n.-171C>G
ENST00000697695.1:n.788C>G
ENST00000337432.9:c.181C>G MANE Select	ENSP00000336701.4:p.Leu61Val
ENST00000337432.8:c.181C>G	ENSP00000336701.4:p.Leu61Val
ENST00000421782.3:c.181C>G	ENSP00000391450.2:p.Leu61Val
ENST00000461271.5:c.-171C>G	ENSP00000464056.1:n.-171C>G
ENST00000475762.5:c.*884C>G	ENSP00000432421.1:n.*884C>G
ENST00000482007.5:c.181C>G	ENSP00000433332.1:p.Leu61Val
ENST00000486827.1:c.*1045C>G	ENSP00000436761.1:n.*1045C>G
ENST00000487525.5:c.181C>G	ENSP00000431637.1:p.Leu61Val
ENST00000487921.5:n.93C>G
ENST00000583539.5:c.181C>G	ENSP00000463121.1:p.Leu61Val
ENST00000584617.5:c.127-1727C>G
NM_002876.3:c.181C>G	NP_002867.1:p.Leu61Val
NM_058216.2:c.181C>G	NP_478123.1:p.Leu61Val
NR_103872.1:n.252C>G
NR_103873.1:n.149C>G
XM_006722001.2:c.181C>G	XP_006722064.1:p.Leu61Val
XM_006722002.2:c.181C>G	XP_006722065.1:p.Leu61Val
XM_006722004.2:c.-171C>G	XP_006722067.1:n.-171C>G
XM_006722005.2:c.-171C>G	XP_006722068.1:n.-171C>G
XM_011525092.1:c.-171C>G	XP_011523394.1:n.-171C>G
XM_011525093.1:c.-171C>G	XP_011523395.1:n.-171C>G
XM_011525094.1:c.-171C>G	XP_011523396.1:n.-171C>G
XR_934513.1:n.254C>G
XR_934514.1:n.254C>G
XM_006722001.4:c.181C>G	XP_006722064.1:p.Leu61Val
XM_006722002.4:c.181C>G	XP_006722065.1:p.Leu61Val
XM_006722004.3:c.-171C>G	XP_006722067.1:n.-171C>G
XM_006722005.3:c.-171C>G	XP_006722068.1:n.-171C>G
XM_011525092.2:c.-171C>G	XP_011523394.1:n.-171C>G
XM_011525093.2:c.-171C>G	XP_011523395.1:n.-171C>G
XM_011525094.2:c.-171C>G	XP_011523396.1:n.-171C>G
XM_017024914.1:c.-171C>G	XP_016880403.1:n.-171C>G
XM_017024915.1:c.-171C>G	XP_016880404.1:n.-171C>G
XM_017024916.1:c.-171C>G	XP_016880405.1:n.-171C>G
XM_017024917.1:c.-171C>G	XP_016880406.1:n.-171C>G
XM_017024918.2:c.-171C>G	XP_016880407.1:n.-171C>G
XM_017024919.1:c.-171C>G	XP_016880408.1:n.-171C>G
XR_934513.3:n.685C>G
XR_934514.3:n.685C>G
NM_058216.3:c.181C>G MANE Select	NP_478123.1:p.Leu61Val
NR_103872.2:n.223C>G
NM_002876.4:c.181C>G	NP_002867.1:p.Leu61Val