Canonical Allele Identifier: CA400365051
Community Standard Title: NM_058216.3(RAD51C):c.1003T>G (p.Cys335Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732521T>G , CM000679.2:g.58732521T>G GRCh38
NC_000017.10:g.56809882T>G , CM000679.1:g.56809882T>G GRCh37
NC_000017.9:g.54164881T>G NCBI36
NG_023199.1:g.44920T>G , LRG_314:g.44920T>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.1003T>G MANE Select NP_478123.1:p.Cys335Gly
ENST00000337432.9:c.1003T>G MANE Select ENSP00000336701.4:p.Cys335Gly
NM_058216.2:c.1003T>G NP_478123.1:p.Cys335Gly
NR_103872.1:n.907T>G
NR_103872.2:n.878T>G
ENST00000337432.8:c.1003T>G ENSP00000336701.4:p.Cys335Gly
ENST00000413590.5:c.644T>G
ENST00000461271.6:c.652T>G ENSP00000464056.2:p.Cys218Gly
ENST00000461706.1:n.190T>G
ENST00000475762.5:c.*1639T>G ENSP00000432421.1:n.*1639T>G
ENST00000482007.5:c.*431T>G ENSP00000433332.1:n.*431T>G
ENST00000487525.5:c.*579T>G ENSP00000431637.1:n.*579T>G
ENST00000578151.1:n.240-1597T>G
ENST00000581221.5:n.518T>G
ENST00000583539.5:c.1003T>G ENSP00000463121.1:p.Cys335Gly
ENST00000584804.1:c.237T>G ENSP00000463658.1:p.Asn79Lys
ENST00000697680.1:c.*1967T>G ENSP00000513392.1:n.*1967T>G
ENST00000697681.1:c.*2164T>G ENSP00000513393.1:n.*2164T>G
ENST00000697683.1:c.*1939T>G ENSP00000513395.1:n.*1939T>G
ENST00000697685.1:c.*1700T>G ENSP00000513396.1:n.*1700T>G
ENST00000697686.1:c.774T>G ENSP00000513397.1:p.Asn258Lys
ENST00000697689.1:c.*1441-1597T>G ENSP00000513398.1:n.*1441-1597T>G
ENST00000697690.1:c.905-1597T>G ENSP00000513399.1:n.905-1597T>G
ENST00000697691.1:c.*975T>G ENSP00000513400.1:n.*975T>G
ENST00000697692.1:c.*1015T>G ENSP00000513401.1:n.*1015T>G
ENST00000697694.1:c.652T>G ENSP00000513402.1:p.Cys218Gly
ENST00000697695.1:n.1610T>G
XM_006722001.2:c.1006T>G XP_006722064.1:p.Cys336Gly
XM_006722001.4:c.1006T>G XP_006722064.1:p.Cys336Gly
XM_006722002.2:c.942T>G XP_006722065.1:p.Asn314Lys
XM_006722002.4:c.942T>G XP_006722065.1:p.Asn314Lys
XM_006722004.2:c.655T>G XP_006722067.1:p.Cys219Gly
XM_006722004.3:c.655T>G XP_006722067.1:p.Cys219Gly
XM_006722005.2:c.655T>G XP_006722068.1:p.Cys219Gly
XM_006722005.3:c.655T>G XP_006722068.1:p.Cys219Gly
XM_011525092.1:c.655T>G XP_011523394.1:p.Cys219Gly
XM_011525092.2:c.655T>G XP_011523394.1:p.Cys219Gly
XM_011525093.1:c.655T>G XP_011523395.1:p.Cys219Gly
XM_011525093.2:c.655T>G XP_011523395.1:p.Cys219Gly
XM_011525094.1:c.655T>G XP_011523396.1:p.Cys219Gly
XM_011525094.2:c.655T>G XP_011523396.1:p.Cys219Gly
XM_017024914.1:c.652T>G XP_016880403.1:p.Cys218Gly
XM_017024915.1:c.652T>G XP_016880404.1:p.Cys218Gly
XM_017024916.1:c.652T>G XP_016880405.1:p.Cys218Gly
XM_017024917.1:c.652T>G XP_016880406.1:p.Cys218Gly
XM_017024918.2:c.652T>G XP_016880407.1:p.Cys218Gly
XM_017024919.1:c.591T>G XP_016880408.1:p.Asn197Lys
XR_934513.1:n.1221T>G
XR_934513.3:n.1652T>G
XR_934514.1:n.1224T>G
XR_934514.3:n.1655T>G
XR_934886.1:n.149+5550A>C
XR_934886.2:n.149+5550A>C