Canonical Allele Identifier: CA400366239
Community Standard Title: NM_058216.3(RAD51C):c.1072C>T (p.Gln358Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58734163C>T , CM000679.2:g.58734163C>T GRCh38
NC_000017.10:g.56811524C>T , CM000679.1:g.56811524C>T GRCh37
NC_000017.9:g.54166523C>T NCBI36
NG_023199.1:g.46562C>T , LRG_314:g.46562C>T

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1072C>T MANE Select NP_478123.1:p.Gln358Ter
ENST00000337432.9:c.1072C>T MANE Select ENSP00000336701.4:p.Gln358Ter
NM_058216.2:c.1072C>T NP_478123.1:p.Gln358Ter
NR_103872.1:n.976C>T
NR_103872.2:n.947C>T
ENST00000337432.8:c.1072C>T ENSP00000336701.4:p.Gln358Ter
ENST00000413590.5:c.713C>T
ENST00000461271.6:c.*1604C>T ENSP00000464056.2:n.*1604C>T
ENST00000461706.1:n.259C>T
ENST00000475762.5:c.*1708C>T ENSP00000432421.1:n.*1708C>T
ENST00000482007.5:c.*500C>T ENSP00000433332.1:n.*500C>T
ENST00000487525.5:c.*648C>T ENSP00000431637.1:n.*648C>T
ENST00000578151.1:n.285C>T
ENST00000581221.5:n.587C>T
ENST00000584804.1:c.306C>T ENSP00000463658.1:p.Cys102=
ENST00000697680.1:c.*2036C>T ENSP00000513392.1:n.*2036C>T
ENST00000697681.1:c.*2233C>T ENSP00000513393.1:n.*2233C>T
ENST00000697683.1:c.*2008C>T ENSP00000513395.1:n.*2008C>T
ENST00000697685.1:c.*1769C>T ENSP00000513396.1:n.*1769C>T
ENST00000697686.1:c.843C>T ENSP00000513397.1:p.Cys281=
ENST00000697689.1:c.*1486C>T ENSP00000513398.1:n.*1486C>T
ENST00000697690.1:c.*32C>T ENSP00000513399.1:n.*32C>T
ENST00000697691.1:c.*1044C>T ENSP00000513400.1:n.*1044C>T
ENST00000697692.1:c.*1084C>T ENSP00000513401.1:n.*1084C>T
ENST00000697694.1:c.721C>T ENSP00000513402.1:p.Gln241Ter
ENST00000697695.1:n.1679C>T
XM_006722001.2:c.1075C>T XP_006722064.1:p.Gln359Ter
XM_006722001.4:c.1075C>T XP_006722064.1:p.Gln359Ter
XM_006722002.2:c.1011C>T XP_006722065.1:p.Cys337=
XM_006722002.4:c.1011C>T XP_006722065.1:p.Cys337=
XM_006722004.2:c.724C>T XP_006722067.1:p.Gln242Ter
XM_006722004.3:c.724C>T XP_006722067.1:p.Gln242Ter
XM_006722005.2:c.724C>T XP_006722068.1:p.Gln242Ter
XM_006722005.3:c.724C>T XP_006722068.1:p.Gln242Ter
XM_011525092.1:c.724C>T XP_011523394.1:p.Gln242Ter
XM_011525092.2:c.724C>T XP_011523394.1:p.Gln242Ter
XM_011525093.1:c.724C>T XP_011523395.1:p.Gln242Ter
XM_011525093.2:c.724C>T XP_011523395.1:p.Gln242Ter
XM_011525094.1:c.724C>T XP_011523396.1:p.Gln242Ter
XM_011525094.2:c.724C>T XP_011523396.1:p.Gln242Ter
XM_017024914.1:c.721C>T XP_016880403.1:p.Gln241Ter
XM_017024915.1:c.721C>T XP_016880404.1:p.Gln241Ter
XM_017024916.1:c.721C>T XP_016880405.1:p.Gln241Ter
XM_017024917.1:c.721C>T XP_016880406.1:p.Gln241Ter
XM_017024918.2:c.721C>T XP_016880407.1:p.Gln241Ter
XM_017024919.1:c.660C>T XP_016880408.1:p.Cys220=
XR_934513.1:n.1290C>T
XR_934513.3:n.1721C>T
XR_934514.1:n.1293C>T
XR_934514.3:n.1724C>T
XR_934886.1:n.149+3908G>A
XR_934886.2:n.149+3908G>A