Canonical Allele Identifier: CA196632

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58734200G>A , CM000679.2:g.58734200G>A	GRCh38
NC_000017.10:g.56811561G>A , CM000679.1:g.56811561G>A	GRCh37
NC_000017.9:g.54166560G>A	NCBI36
NG_023199.1:g.46599G>A , LRG_314:g.46599G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.1109G>A MANE Select	NP_478123.1:p.Arg370Gln
ENST00000337432.9:c.1109G>A MANE Select	ENSP00000336701.4:p.Arg370Gln
NM_058216.2:c.1109G>A	NP_478123.1:p.Arg370Gln
NR_103872.1:n.1013G>A
NR_103872.2:n.984G>A
ENST00000337432.8:c.1109G>A	ENSP00000336701.4:p.Arg370Gln
ENST00000413590.5:c.750G>A
ENST00000461271.6:c.*1641G>A	ENSP00000464056.2:n.*1641G>A
ENST00000461706.1:n.296G>A
ENST00000475762.5:c.*1745G>A	ENSP00000432421.1:n.*1745G>A
ENST00000482007.5:c.*537G>A	ENSP00000433332.1:n.*537G>A
ENST00000487525.5:c.*685G>A	ENSP00000431637.1:n.*685G>A
ENST00000578151.1:n.322G>A
ENST00000581221.5:n.624G>A
ENST00000584804.1:c.343G>A	ENSP00000463658.1:n.343G>A
ENST00000697680.1:c.*2073G>A	ENSP00000513392.1:n.*2073G>A
ENST00000697681.1:c.*2270G>A	ENSP00000513393.1:n.*2270G>A
ENST00000697683.1:c.*2045G>A	ENSP00000513395.1:n.*2045G>A
ENST00000697685.1:c.*1806G>A	ENSP00000513396.1:n.*1806G>A
ENST00000697686.1:c.*19G>A	ENSP00000513397.1:n.*19G>A
ENST00000697689.1:c.*1523G>A	ENSP00000513398.1:n.*1523G>A
ENST00000697690.1:c.*69G>A	ENSP00000513399.1:n.*69G>A
ENST00000697691.1:c.*1081G>A	ENSP00000513400.1:n.*1081G>A
ENST00000697692.1:c.*1121G>A	ENSP00000513401.1:n.*1121G>A
ENST00000697694.1:c.758G>A	ENSP00000513402.1:p.Arg253Gln
ENST00000697695.1:n.1716G>A
XM_006722001.2:c.1112G>A	XP_006722064.1:p.Arg371Gln
XM_006722001.4:c.1112G>A	XP_006722064.1:p.Arg371Gln
XM_006722002.2:c.*19G>A	XP_006722065.1:n.*19G>A
XM_006722002.4:c.*19G>A	XP_006722065.1:n.*19G>A
XM_006722004.2:c.761G>A	XP_006722067.1:p.Arg254Gln
XM_006722004.3:c.761G>A	XP_006722067.1:p.Arg254Gln
XM_006722005.2:c.761G>A	XP_006722068.1:p.Arg254Gln
XM_006722005.3:c.761G>A	XP_006722068.1:p.Arg254Gln
XM_011525092.1:c.761G>A	XP_011523394.1:p.Arg254Gln
XM_011525092.2:c.761G>A	XP_011523394.1:p.Arg254Gln
XM_011525093.1:c.761G>A	XP_011523395.1:p.Arg254Gln
XM_011525093.2:c.761G>A	XP_011523395.1:p.Arg254Gln
XM_011525094.1:c.761G>A	XP_011523396.1:p.Arg254Gln
XM_011525094.2:c.761G>A	XP_011523396.1:p.Arg254Gln
XM_017024914.1:c.758G>A	XP_016880403.1:p.Arg253Gln
XM_017024915.1:c.758G>A	XP_016880404.1:p.Arg253Gln
XM_017024916.1:c.758G>A	XP_016880405.1:p.Arg253Gln
XM_017024917.1:c.758G>A	XP_016880406.1:p.Arg253Gln
XM_017024918.2:c.758G>A	XP_016880407.1:p.Arg253Gln
XM_017024919.1:c.*19G>A	XP_016880408.1:n.*19G>A
XR_934513.1:n.1327G>A
XR_934513.3:n.1758G>A
XR_934886.1:n.149+3871C>T
XR_934886.2:n.149+3871C>T