Canonical Allele Identifier: CA400353303

Gene: RAD51C

Linked Data

• MyVariant Identifiers: chr17:g.56787240T>G (hg19) ; chr17:g.58709879T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709879T>G , CM000679.2:g.58709879T>G	GRCh38
NC_000017.10:g.56787240T>G , CM000679.1:g.56787240T>G	GRCh37
NC_000017.9:g.54142239T>G	NCBI36
NG_023199.1:g.22278T>G , LRG_314:g.22278T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461271.6:c.375T>G	ENSP00000464056.2:p.Asp125Glu
ENST00000697678.1:n.628T>G
ENST00000697679.1:n.1800T>G
ENST00000697680.1:c.*1590T>G	ENSP00000513392.1:n.*1590T>G
ENST00000697681.1:c.*1887T>G	ENSP00000513393.1:n.*1887T>G
ENST00000697683.1:c.*1590T>G	ENSP00000513395.1:n.*1590T>G
ENST00000697684.1:n.786T>G
ENST00000697685.1:c.*1423T>G	ENSP00000513396.1:n.*1423T>G
ENST00000697686.1:c.375T>G	ENSP00000513397.1:p.Asp125Glu
ENST00000697687.1:n.605T>G
ENST00000697688.1:n.772T>G
ENST00000697689.1:c.*1262T>G	ENSP00000513398.1:n.*1262T>G
ENST00000697690.1:c.726T>G	ENSP00000513399.1:p.Asp242Glu
ENST00000697691.1:c.*698T>G	ENSP00000513400.1:n.*698T>G
ENST00000697692.1:c.*738T>G	ENSP00000513401.1:n.*738T>G
ENST00000697694.1:c.375T>G	ENSP00000513402.1:p.Asp125Glu
ENST00000697695.1:n.1333T>G
ENST00000337432.9:c.726T>G MANE Select	ENSP00000336701.4:p.Asp242Glu
ENST00000337432.8:c.726T>G	ENSP00000336701.4:p.Asp242Glu
ENST00000413590.5:c.364T>G
ENST00000461271.5:c.375T>G	ENSP00000464056.1:p.Asp125Glu
ENST00000475762.5:c.*1429T>G	ENSP00000432421.1:n.*1429T>G
ENST00000482007.5:c.*154T>G	ENSP00000433332.1:n.*154T>G
ENST00000487525.5:c.*299T>G	ENSP00000431637.1:n.*299T>G
ENST00000578151.1:n.61T>G
ENST00000581221.5:n.241T>G
ENST00000583539.5:c.726T>G	ENSP00000463121.1:p.Asp242Glu
ENST00000584617.5:c.448T>G
ENST00000584804.1:c.21T>G	ENSP00000463658.1:p.Asp7Glu
NM_058216.2:c.726T>G	NP_478123.1:p.Asp242Glu
NR_103872.1:n.630T>G
XM_006722001.2:c.726T>G	XP_006722064.1:p.Asp242Glu
XM_006722002.2:c.726T>G	XP_006722065.1:p.Asp242Glu
XM_006722004.2:c.375T>G	XP_006722067.1:p.Asp125Glu
XM_006722005.2:c.375T>G	XP_006722068.1:p.Asp125Glu
XM_011525092.1:c.375T>G	XP_011523394.1:p.Asp125Glu
XM_011525093.1:c.375T>G	XP_011523395.1:p.Asp125Glu
XM_011525094.1:c.375T>G	XP_011523396.1:p.Asp125Glu
XR_934513.1:n.944T>G
XR_934514.1:n.944T>G
XM_006722001.4:c.726T>G	XP_006722064.1:p.Asp242Glu
XM_006722002.4:c.726T>G	XP_006722065.1:p.Asp242Glu
XM_006722004.3:c.375T>G	XP_006722067.1:p.Asp125Glu
XM_006722005.3:c.375T>G	XP_006722068.1:p.Asp125Glu
XM_011525092.2:c.375T>G	XP_011523394.1:p.Asp125Glu
XM_011525093.2:c.375T>G	XP_011523395.1:p.Asp125Glu
XM_011525094.2:c.375T>G	XP_011523396.1:p.Asp125Glu
XM_017024914.1:c.375T>G	XP_016880403.1:p.Asp125Glu
XM_017024915.1:c.375T>G	XP_016880404.1:p.Asp125Glu
XM_017024916.1:c.375T>G	XP_016880405.1:p.Asp125Glu
XM_017024917.1:c.375T>G	XP_016880406.1:p.Asp125Glu
XM_017024918.2:c.375T>G	XP_016880407.1:p.Asp125Glu
XM_017024919.1:c.375T>G	XP_016880408.1:p.Asp125Glu
XR_934513.3:n.1375T>G
XR_934514.3:n.1375T>G
NM_058216.3:c.726T>G MANE Select	NP_478123.1:p.Asp242Glu
NR_103872.2:n.601T>G