Canonical Allele Identifier: CA197766
Community Standard Title: NM_058216.3(RAD51C):c.1055C>A (p.Thr352Asn)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734146C>A , CM000679.2:g.58734146C>A GRCh38
NC_000017.10:g.56811507C>A , CM000679.1:g.56811507C>A GRCh37
NC_000017.9:g.54166506C>A NCBI36
NG_023199.1:g.46545C>A , LRG_314:g.46545C>A

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1055C>A MANE Select NP_478123.1:p.Thr352Asn
ENST00000337432.9:c.1055C>A MANE Select ENSP00000336701.4:p.Thr352Asn
NM_058216.2:c.1055C>A NP_478123.1:p.Thr352Asn
NR_103872.1:n.959C>A
NR_103872.2:n.930C>A
ENST00000337432.8:c.1055C>A ENSP00000336701.4:p.Thr352Asn
ENST00000413590.5:c.696C>A
ENST00000461271.6:c.*1587C>A ENSP00000464056.2:n.*1587C>A
ENST00000461706.1:n.242C>A
ENST00000475762.5:c.*1691C>A ENSP00000432421.1:n.*1691C>A
ENST00000482007.5:c.*483C>A ENSP00000433332.1:n.*483C>A
ENST00000487525.5:c.*631C>A ENSP00000431637.1:n.*631C>A
ENST00000578151.1:n.268C>A
ENST00000581221.5:n.570C>A
ENST00000584804.1:c.289C>A ENSP00000463658.1:p.Leu97Ile
ENST00000697680.1:c.*2019C>A ENSP00000513392.1:n.*2019C>A
ENST00000697681.1:c.*2216C>A ENSP00000513393.1:n.*2216C>A
ENST00000697683.1:c.*1991C>A ENSP00000513395.1:n.*1991C>A
ENST00000697685.1:c.*1752C>A ENSP00000513396.1:n.*1752C>A
ENST00000697686.1:c.826C>A ENSP00000513397.1:p.Leu276Ile
ENST00000697689.1:c.*1469C>A ENSP00000513398.1:n.*1469C>A
ENST00000697690.1:c.*15C>A ENSP00000513399.1:n.*15C>A
ENST00000697691.1:c.*1027C>A ENSP00000513400.1:n.*1027C>A
ENST00000697692.1:c.*1067C>A ENSP00000513401.1:n.*1067C>A
ENST00000697694.1:c.704C>A ENSP00000513402.1:p.Thr235Asn
ENST00000697695.1:n.1662C>A
XM_006722001.2:c.1058C>A XP_006722064.1:p.Thr353Asn
XM_006722001.4:c.1058C>A XP_006722064.1:p.Thr353Asn
XM_006722002.2:c.994C>A XP_006722065.1:p.Leu332Ile
XM_006722002.4:c.994C>A XP_006722065.1:p.Leu332Ile
XM_006722004.2:c.707C>A XP_006722067.1:p.Thr236Asn
XM_006722004.3:c.707C>A XP_006722067.1:p.Thr236Asn
XM_006722005.2:c.707C>A XP_006722068.1:p.Thr236Asn
XM_006722005.3:c.707C>A XP_006722068.1:p.Thr236Asn
XM_011525092.1:c.707C>A XP_011523394.1:p.Thr236Asn
XM_011525092.2:c.707C>A XP_011523394.1:p.Thr236Asn
XM_011525093.1:c.707C>A XP_011523395.1:p.Thr236Asn
XM_011525093.2:c.707C>A XP_011523395.1:p.Thr236Asn
XM_011525094.1:c.707C>A XP_011523396.1:p.Thr236Asn
XM_011525094.2:c.707C>A XP_011523396.1:p.Thr236Asn
XM_017024914.1:c.704C>A XP_016880403.1:p.Thr235Asn
XM_017024915.1:c.704C>A XP_016880404.1:p.Thr235Asn
XM_017024916.1:c.704C>A XP_016880405.1:p.Thr235Asn
XM_017024917.1:c.704C>A XP_016880406.1:p.Thr235Asn
XM_017024918.2:c.704C>A XP_016880407.1:p.Thr235Asn
XM_017024919.1:c.643C>A XP_016880408.1:p.Leu215Ile
XR_934513.1:n.1273C>A
XR_934513.3:n.1704C>A
XR_934514.1:n.1276C>A
XR_934514.3:n.1707C>A
XR_934886.1:n.149+3925G>T
XR_934886.2:n.149+3925G>T