Canonical Allele Identifier: CA400364904
Community Standard Title: NM_058216.3(RAD51C):c.981C>G (p.Tyr327Ter)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58732499C>G , CM000679.2:g.58732499C>G GRCh38
NC_000017.10:g.56809860C>G , CM000679.1:g.56809860C>G GRCh37
NC_000017.9:g.54164859C>G NCBI36
NG_023199.1:g.44898C>G , LRG_314:g.44898C>G

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.981C>G MANE Select NP_478123.1:p.Tyr327Ter
ENST00000337432.9:c.981C>G MANE Select ENSP00000336701.4:p.Tyr327Ter
NM_058216.2:c.981C>G NP_478123.1:p.Tyr327Ter
NR_103872.1:n.885C>G
NR_103872.2:n.856C>G
ENST00000337432.8:c.981C>G ENSP00000336701.4:p.Tyr327Ter
ENST00000413590.5:c.622C>G
ENST00000461271.6:c.630C>G ENSP00000464056.2:p.Tyr210Ter
ENST00000461706.1:n.168C>G
ENST00000475762.5:c.*1617C>G ENSP00000432421.1:n.*1617C>G
ENST00000482007.5:c.*409C>G ENSP00000433332.1:n.*409C>G
ENST00000487525.5:c.*557C>G ENSP00000431637.1:n.*557C>G
ENST00000578151.1:n.240-1619C>G
ENST00000581221.5:n.496C>G
ENST00000583539.5:c.981C>G ENSP00000463121.1:p.Tyr327Ter
ENST00000584617.5:c.703C>G
ENST00000584804.1:c.215C>G ENSP00000463658.1:p.Thr72Arg
ENST00000697680.1:c.*1945C>G ENSP00000513392.1:n.*1945C>G
ENST00000697681.1:c.*2142C>G ENSP00000513393.1:n.*2142C>G
ENST00000697683.1:c.*1917C>G ENSP00000513395.1:n.*1917C>G
ENST00000697685.1:c.*1678C>G ENSP00000513396.1:n.*1678C>G
ENST00000697686.1:c.752C>G ENSP00000513397.1:p.Thr251Arg
ENST00000697689.1:c.*1441-1619C>G ENSP00000513398.1:n.*1441-1619C>G
ENST00000697690.1:c.905-1619C>G ENSP00000513399.1:n.905-1619C>G
ENST00000697691.1:c.*953C>G ENSP00000513400.1:n.*953C>G
ENST00000697692.1:c.*993C>G ENSP00000513401.1:n.*993C>G
ENST00000697694.1:c.630C>G ENSP00000513402.1:p.Tyr210Ter
ENST00000697695.1:n.1588C>G
XM_006722001.2:c.984C>G XP_006722064.1:p.Tyr328Ter
XM_006722001.4:c.984C>G XP_006722064.1:p.Tyr328Ter
XM_006722002.2:c.920C>G XP_006722065.1:p.Thr307Arg
XM_006722002.4:c.920C>G XP_006722065.1:p.Thr307Arg
XM_006722004.2:c.633C>G XP_006722067.1:p.Tyr211Ter
XM_006722004.3:c.633C>G XP_006722067.1:p.Tyr211Ter
XM_006722005.2:c.633C>G XP_006722068.1:p.Tyr211Ter
XM_006722005.3:c.633C>G XP_006722068.1:p.Tyr211Ter
XM_011525092.1:c.633C>G XP_011523394.1:p.Tyr211Ter
XM_011525092.2:c.633C>G XP_011523394.1:p.Tyr211Ter
XM_011525093.1:c.633C>G XP_011523395.1:p.Tyr211Ter
XM_011525093.2:c.633C>G XP_011523395.1:p.Tyr211Ter
XM_011525094.1:c.633C>G XP_011523396.1:p.Tyr211Ter
XM_011525094.2:c.633C>G XP_011523396.1:p.Tyr211Ter
XM_017024914.1:c.630C>G XP_016880403.1:p.Tyr210Ter
XM_017024915.1:c.630C>G XP_016880404.1:p.Tyr210Ter
XM_017024916.1:c.630C>G XP_016880405.1:p.Tyr210Ter
XM_017024917.1:c.630C>G XP_016880406.1:p.Tyr210Ter
XM_017024918.2:c.630C>G XP_016880407.1:p.Tyr210Ter
XM_017024919.1:c.569C>G XP_016880408.1:p.Thr190Arg
XR_934513.1:n.1199C>G
XR_934513.3:n.1630C>G
XR_934514.1:n.1202C>G
XR_934514.3:n.1633C>G
XR_934886.1:n.149+5572G>C
XR_934886.2:n.149+5572G>C