Canonical Allele Identifier: CA8677408
Community Standard Title: NM_058216.3(RAD51C):c.1046C>T (p.Thr349Ile)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734137C>T , CM000679.2:g.58734137C>T GRCh38
NC_000017.10:g.56811498C>T , CM000679.1:g.56811498C>T GRCh37
NC_000017.9:g.54166497C>T NCBI36
NG_023199.1:g.46536C>T , LRG_314:g.46536C>T

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1046C>T MANE Select NP_478123.1:p.Thr349Ile
ENST00000337432.9:c.1046C>T MANE Select ENSP00000336701.4:p.Thr349Ile
NM_058216.2:c.1046C>T NP_478123.1:p.Thr349Ile
NR_103872.1:n.950C>T
NR_103872.2:n.921C>T
ENST00000337432.8:c.1046C>T ENSP00000336701.4:p.Thr349Ile
ENST00000413590.5:c.687C>T
ENST00000461271.6:c.*1578C>T ENSP00000464056.2:n.*1578C>T
ENST00000461706.1:n.233C>T
ENST00000475762.5:c.*1682C>T ENSP00000432421.1:n.*1682C>T
ENST00000482007.5:c.*474C>T ENSP00000433332.1:n.*474C>T
ENST00000487525.5:c.*622C>T ENSP00000431637.1:n.*622C>T
ENST00000578151.1:n.259C>T
ENST00000581221.5:n.561C>T
ENST00000584804.1:c.280C>T ENSP00000463658.1:p.Leu94=
ENST00000697680.1:c.*2010C>T ENSP00000513392.1:n.*2010C>T
ENST00000697681.1:c.*2207C>T ENSP00000513393.1:n.*2207C>T
ENST00000697683.1:c.*1982C>T ENSP00000513395.1:n.*1982C>T
ENST00000697685.1:c.*1743C>T ENSP00000513396.1:n.*1743C>T
ENST00000697686.1:c.817C>T ENSP00000513397.1:p.Leu273=
ENST00000697689.1:c.*1460C>T ENSP00000513398.1:n.*1460C>T
ENST00000697690.1:c.*6C>T ENSP00000513399.1:n.*6C>T
ENST00000697691.1:c.*1018C>T ENSP00000513400.1:n.*1018C>T
ENST00000697692.1:c.*1058C>T ENSP00000513401.1:n.*1058C>T
ENST00000697694.1:c.695C>T ENSP00000513402.1:p.Thr232Ile
ENST00000697695.1:n.1653C>T
XM_006722001.2:c.1049C>T XP_006722064.1:p.Thr350Ile
XM_006722001.4:c.1049C>T XP_006722064.1:p.Thr350Ile
XM_006722002.2:c.985C>T XP_006722065.1:p.Leu329=
XM_006722002.4:c.985C>T XP_006722065.1:p.Leu329=
XM_006722004.2:c.698C>T XP_006722067.1:p.Thr233Ile
XM_006722004.3:c.698C>T XP_006722067.1:p.Thr233Ile
XM_006722005.2:c.698C>T XP_006722068.1:p.Thr233Ile
XM_006722005.3:c.698C>T XP_006722068.1:p.Thr233Ile
XM_011525092.1:c.698C>T XP_011523394.1:p.Thr233Ile
XM_011525092.2:c.698C>T XP_011523394.1:p.Thr233Ile
XM_011525093.1:c.698C>T XP_011523395.1:p.Thr233Ile
XM_011525093.2:c.698C>T XP_011523395.1:p.Thr233Ile
XM_011525094.1:c.698C>T XP_011523396.1:p.Thr233Ile
XM_011525094.2:c.698C>T XP_011523396.1:p.Thr233Ile
XM_017024914.1:c.695C>T XP_016880403.1:p.Thr232Ile
XM_017024915.1:c.695C>T XP_016880404.1:p.Thr232Ile
XM_017024916.1:c.695C>T XP_016880405.1:p.Thr232Ile
XM_017024917.1:c.695C>T XP_016880406.1:p.Thr232Ile
XM_017024918.2:c.695C>T XP_016880407.1:p.Thr232Ile
XM_017024919.1:c.634C>T XP_016880408.1:p.Leu212=
XR_934513.1:n.1264C>T
XR_934513.3:n.1695C>T
XR_934514.1:n.1267C>T
XR_934514.3:n.1698C>T
XR_934886.1:n.149+3934G>A
XR_934886.2:n.149+3934G>A