Canonical Allele Identifier: CA400365920

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58734129T>A , CM000679.2:g.58734129T>A	GRCh38
NC_000017.10:g.56811490T>A , CM000679.1:g.56811490T>A	GRCh37
NC_000017.9:g.54166489T>A	NCBI36
NG_023199.1:g.46528T>A , LRG_314:g.46528T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.1038T>A MANE Select	NP_478123.1:p.Phe346Leu
ENST00000337432.9:c.1038T>A MANE Select	ENSP00000336701.4:p.Phe346Leu
NM_058216.2:c.1038T>A	NP_478123.1:p.Phe346Leu
NR_103872.1:n.942T>A
NR_103872.2:n.913T>A
ENST00000337432.8:c.1038T>A	ENSP00000336701.4:p.Phe346Leu
ENST00000413590.5:c.679T>A
ENST00000461271.6:c.*1570T>A	ENSP00000464056.2:n.*1570T>A
ENST00000461706.1:n.225T>A
ENST00000475762.5:c.*1674T>A	ENSP00000432421.1:n.*1674T>A
ENST00000482007.5:c.*466T>A	ENSP00000433332.1:n.*466T>A
ENST00000487525.5:c.*614T>A	ENSP00000431637.1:n.*614T>A
ENST00000578151.1:n.251T>A
ENST00000581221.5:n.553T>A
ENST00000584804.1:c.272T>A	ENSP00000463658.1:p.Leu91Ter
ENST00000697680.1:c.*2002T>A	ENSP00000513392.1:n.*2002T>A
ENST00000697681.1:c.*2199T>A	ENSP00000513393.1:n.*2199T>A
ENST00000697683.1:c.*1974T>A	ENSP00000513395.1:n.*1974T>A
ENST00000697685.1:c.*1735T>A	ENSP00000513396.1:n.*1735T>A
ENST00000697686.1:c.809T>A	ENSP00000513397.1:p.Leu270Ter
ENST00000697689.1:c.*1452T>A	ENSP00000513398.1:n.*1452T>A
ENST00000697690.1:c.916T>A	ENSP00000513399.1:p.Ter306Lys
ENST00000697691.1:c.*1010T>A	ENSP00000513400.1:n.*1010T>A
ENST00000697692.1:c.*1050T>A	ENSP00000513401.1:n.*1050T>A
ENST00000697694.1:c.687T>A	ENSP00000513402.1:p.Phe229Leu
ENST00000697695.1:n.1645T>A
XM_006722001.2:c.1041T>A	XP_006722064.1:p.Phe347Leu
XM_006722001.4:c.1041T>A	XP_006722064.1:p.Phe347Leu
XM_006722002.2:c.977T>A	XP_006722065.1:p.Leu326Ter
XM_006722002.4:c.977T>A	XP_006722065.1:p.Leu326Ter
XM_006722004.2:c.690T>A	XP_006722067.1:p.Phe230Leu
XM_006722004.3:c.690T>A	XP_006722067.1:p.Phe230Leu
XM_006722005.2:c.690T>A	XP_006722068.1:p.Phe230Leu
XM_006722005.3:c.690T>A	XP_006722068.1:p.Phe230Leu
XM_011525092.1:c.690T>A	XP_011523394.1:p.Phe230Leu
XM_011525092.2:c.690T>A	XP_011523394.1:p.Phe230Leu
XM_011525093.1:c.690T>A	XP_011523395.1:p.Phe230Leu
XM_011525093.2:c.690T>A	XP_011523395.1:p.Phe230Leu
XM_011525094.1:c.690T>A	XP_011523396.1:p.Phe230Leu
XM_011525094.2:c.690T>A	XP_011523396.1:p.Phe230Leu
XM_017024914.1:c.687T>A	XP_016880403.1:p.Phe229Leu
XM_017024915.1:c.687T>A	XP_016880404.1:p.Phe229Leu
XM_017024916.1:c.687T>A	XP_016880405.1:p.Phe229Leu
XM_017024917.1:c.687T>A	XP_016880406.1:p.Phe229Leu
XM_017024918.2:c.687T>A	XP_016880407.1:p.Phe229Leu
XM_017024919.1:c.626T>A	XP_016880408.1:p.Leu209Ter
XR_934513.1:n.1256T>A
XR_934513.3:n.1687T>A
XR_934514.1:n.1259T>A
XR_934514.3:n.1690T>A
XR_934886.1:n.149+3942A>T
XR_934886.2:n.149+3942A>T