Canonical Allele Identifier: CA292074358
Community Standard Title: NM_058216.3(RAD51C):c.1076C>T (p.Thr359Ile)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734167C>T , CM000679.2:g.58734167C>T GRCh38
NC_000017.10:g.56811528C>T , CM000679.1:g.56811528C>T GRCh37
NC_000017.9:g.54166527C>T NCBI36
NG_023199.1:g.46566C>T , LRG_314:g.46566C>T

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1076C>T MANE Select NP_478123.1:p.Thr359Ile
ENST00000337432.9:c.1076C>T MANE Select ENSP00000336701.4:p.Thr359Ile
NM_058216.2:c.1076C>T NP_478123.1:p.Thr359Ile
NR_103872.1:n.980C>T
NR_103872.2:n.951C>T
ENST00000337432.8:c.1076C>T ENSP00000336701.4:p.Thr359Ile
ENST00000413590.5:c.717C>T
ENST00000461271.6:c.*1608C>T ENSP00000464056.2:n.*1608C>T
ENST00000461706.1:n.263C>T
ENST00000475762.5:c.*1712C>T ENSP00000432421.1:n.*1712C>T
ENST00000482007.5:c.*504C>T ENSP00000433332.1:n.*504C>T
ENST00000487525.5:c.*652C>T ENSP00000431637.1:n.*652C>T
ENST00000578151.1:n.289C>T
ENST00000581221.5:n.591C>T
ENST00000584804.1:c.310C>T ENSP00000463658.1:p.Gln104Ter
ENST00000697680.1:c.*2040C>T ENSP00000513392.1:n.*2040C>T
ENST00000697681.1:c.*2237C>T ENSP00000513393.1:n.*2237C>T
ENST00000697683.1:c.*2012C>T ENSP00000513395.1:n.*2012C>T
ENST00000697685.1:c.*1773C>T ENSP00000513396.1:n.*1773C>T
ENST00000697686.1:c.847C>T ENSP00000513397.1:p.Gln283Ter
ENST00000697689.1:c.*1490C>T ENSP00000513398.1:n.*1490C>T
ENST00000697690.1:c.*36C>T ENSP00000513399.1:n.*36C>T
ENST00000697691.1:c.*1048C>T ENSP00000513400.1:n.*1048C>T
ENST00000697692.1:c.*1088C>T ENSP00000513401.1:n.*1088C>T
ENST00000697694.1:c.725C>T ENSP00000513402.1:p.Thr242Ile
ENST00000697695.1:n.1683C>T
XM_006722001.2:c.1079C>T XP_006722064.1:p.Thr360Ile
XM_006722001.4:c.1079C>T XP_006722064.1:p.Thr360Ile
XM_006722002.2:c.1015C>T XP_006722065.1:p.Gln339Ter
XM_006722002.4:c.1015C>T XP_006722065.1:p.Gln339Ter
XM_006722004.2:c.728C>T XP_006722067.1:p.Thr243Ile
XM_006722004.3:c.728C>T XP_006722067.1:p.Thr243Ile
XM_006722005.2:c.728C>T XP_006722068.1:p.Thr243Ile
XM_006722005.3:c.728C>T XP_006722068.1:p.Thr243Ile
XM_011525092.1:c.728C>T XP_011523394.1:p.Thr243Ile
XM_011525092.2:c.728C>T XP_011523394.1:p.Thr243Ile
XM_011525093.1:c.728C>T XP_011523395.1:p.Thr243Ile
XM_011525093.2:c.728C>T XP_011523395.1:p.Thr243Ile
XM_011525094.1:c.728C>T XP_011523396.1:p.Thr243Ile
XM_011525094.2:c.728C>T XP_011523396.1:p.Thr243Ile
XM_017024914.1:c.725C>T XP_016880403.1:p.Thr242Ile
XM_017024915.1:c.725C>T XP_016880404.1:p.Thr242Ile
XM_017024916.1:c.725C>T XP_016880405.1:p.Thr242Ile
XM_017024917.1:c.725C>T XP_016880406.1:p.Thr242Ile
XM_017024918.2:c.725C>T XP_016880407.1:p.Thr242Ile
XM_017024919.1:c.664C>T XP_016880408.1:p.Gln222Ter
XR_934513.1:n.1294C>T
XR_934513.3:n.1725C>T
XR_934514.1:n.1297C>T
XR_934514.3:n.1728C>T
XR_934886.1:n.149+3904G>A
XR_934886.2:n.149+3904G>A