Canonical Allele Identifier: CA190873
Community Standard Title: NM_058216.3(RAD51C):c.1027C>T (p.Pro343Ser)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734118C>T , CM000679.2:g.58734118C>T GRCh38
NC_000017.10:g.56811479C>T , CM000679.1:g.56811479C>T GRCh37
NC_000017.9:g.54166478C>T NCBI36
NG_023199.1:g.46517C>T , LRG_314:g.46517C>T

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1027C>T MANE Select NP_478123.1:p.Pro343Ser
ENST00000337432.9:c.1027C>T MANE Select ENSP00000336701.4:p.Pro343Ser
NM_058216.2:c.1027C>T NP_478123.1:p.Pro343Ser
NR_103872.1:n.931C>T
NR_103872.2:n.902C>T
ENST00000337432.8:c.1027C>T ENSP00000336701.4:p.Pro343Ser
ENST00000413590.5:c.668C>T
ENST00000461271.6:c.*1559C>T ENSP00000464056.2:n.*1559C>T
ENST00000461706.1:n.214C>T
ENST00000475762.5:c.*1663C>T ENSP00000432421.1:n.*1663C>T
ENST00000482007.5:c.*455C>T ENSP00000433332.1:n.*455C>T
ENST00000487525.5:c.*603C>T ENSP00000431637.1:n.*603C>T
ENST00000578151.1:n.240C>T
ENST00000581221.5:n.542C>T
ENST00000584804.1:c.261C>T ENSP00000463658.1:p.Asn87=
ENST00000697680.1:c.*1991C>T ENSP00000513392.1:n.*1991C>T
ENST00000697681.1:c.*2188C>T ENSP00000513393.1:n.*2188C>T
ENST00000697683.1:c.*1963C>T ENSP00000513395.1:n.*1963C>T
ENST00000697685.1:c.*1724C>T ENSP00000513396.1:n.*1724C>T
ENST00000697686.1:c.798C>T ENSP00000513397.1:p.Asn266=
ENST00000697689.1:c.*1441C>T ENSP00000513398.1:n.*1441C>T
ENST00000697690.1:c.905C>T ENSP00000513399.1:p.Ala302Val
ENST00000697691.1:c.*999C>T ENSP00000513400.1:n.*999C>T
ENST00000697692.1:c.*1039C>T ENSP00000513401.1:n.*1039C>T
ENST00000697694.1:c.676C>T ENSP00000513402.1:p.Pro226Ser
ENST00000697695.1:n.1634C>T
XM_006722001.2:c.1030C>T XP_006722064.1:p.Pro344Ser
XM_006722001.4:c.1030C>T XP_006722064.1:p.Pro344Ser
XM_006722002.2:c.966C>T XP_006722065.1:p.Asn322=
XM_006722002.4:c.966C>T XP_006722065.1:p.Asn322=
XM_006722004.2:c.679C>T XP_006722067.1:p.Pro227Ser
XM_006722004.3:c.679C>T XP_006722067.1:p.Pro227Ser
XM_006722005.2:c.679C>T XP_006722068.1:p.Pro227Ser
XM_006722005.3:c.679C>T XP_006722068.1:p.Pro227Ser
XM_011525092.1:c.679C>T XP_011523394.1:p.Pro227Ser
XM_011525092.2:c.679C>T XP_011523394.1:p.Pro227Ser
XM_011525093.1:c.679C>T XP_011523395.1:p.Pro227Ser
XM_011525093.2:c.679C>T XP_011523395.1:p.Pro227Ser
XM_011525094.1:c.679C>T XP_011523396.1:p.Pro227Ser
XM_011525094.2:c.679C>T XP_011523396.1:p.Pro227Ser
XM_017024914.1:c.676C>T XP_016880403.1:p.Pro226Ser
XM_017024915.1:c.676C>T XP_016880404.1:p.Pro226Ser
XM_017024916.1:c.676C>T XP_016880405.1:p.Pro226Ser
XM_017024917.1:c.676C>T XP_016880406.1:p.Pro226Ser
XM_017024918.2:c.676C>T XP_016880407.1:p.Pro226Ser
XM_017024919.1:c.615C>T XP_016880408.1:p.Asn205=
XR_934513.1:n.1245C>T
XR_934513.3:n.1676C>T
XR_934514.1:n.1248C>T
XR_934514.3:n.1679C>T
XR_934886.1:n.149+3953G>A
XR_934886.2:n.149+3953G>A