Canonical Allele Identifier: CA3057228007
Community Standard Title: NM_058216.3(RAD51C):c.18_19delinsTG (p.Arg7Gly)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58692661_58692662delinsTG , CM000679.2:g.58692661_58692662delinsTG GRCh38
NC_000017.10:g.56770022_56770023delinsTG , CM000679.1:g.56770022_56770023delinsTG GRCh37
NC_000017.9:g.54125021_54125022delinsTG NCBI36
NG_023199.1:g.5060_5061delinsTG , LRG_314:g.5060_5061delinsTG
NG_047169.1:g.4418_4419delinsCA

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.18_19delinsTG MANE Select NP_478123.1:p.Arg7Gly
ENST00000337432.9:c.18_19delinsTG MANE Select ENSP00000336701.4:p.Arg7Gly
NM_002876.3:c.18_19delinsTG NP_002867.1:p.Arg7Gly
NM_002876.4:c.18_19delinsTG NP_002867.1:p.Arg7Gly
NM_058216.2:c.18_19delinsTG NP_478123.1:p.Arg7Gly
NR_103872.1:n.89_90delinsTG
NR_103872.2:n.60_61delinsTG
NR_103873.1:n.89_90delinsTG
ENST00000337432.8:c.18_19delinsTG ENSP00000336701.4:p.Arg7Gly
ENST00000421782.3:c.18_19delinsTG ENSP00000391450.2:p.Arg7Gly
ENST00000461271.5:c.-231_-230delinsTG ENSP00000464056.1:n.-231_-230delinsTG
ENST00000461271.6:c.-231_-230delinsTG ENSP00000464056.2:n.-231_-230delinsTG
ENST00000475762.5:c.18_19delinsTG ENSP00000432421.1:p.Arg7Gly
ENST00000476741.2:n.60_61delinsTG
ENST00000482007.5:c.18_19delinsTG ENSP00000433332.1:p.Arg7Gly
ENST00000486827.1:c.18_19delinsTG ENSP00000436761.1:p.Arg7Gly
ENST00000487525.5:c.18_19delinsTG ENSP00000431637.1:p.Arg7Gly
ENST00000487921.5:n.57+29_57+30delinsTG
ENST00000583539.5:c.18_19delinsTG ENSP00000463121.1:p.Arg7Gly
ENST00000697675.1:n.89_90delinsTG
ENST00000697676.1:n.78_79delinsTG
ENST00000697677.1:n.76_77delinsTG
ENST00000697678.1:n.47+29_47+30delinsTG
ENST00000697679.1:n.69_70delinsTG
ENST00000697680.1:c.18_19delinsTG ENSP00000513392.1:p.Arg7Gly
ENST00000697681.1:c.18_19delinsTG ENSP00000513393.1:p.Arg7Gly
ENST00000697683.1:c.18_19delinsTG ENSP00000513395.1:p.Arg7Gly
ENST00000697684.1:n.78_79delinsTG
ENST00000697685.1:c.18_19delinsTG ENSP00000513396.1:p.Arg7Gly
ENST00000697686.1:c.-207+29_-207+30delinsTG ENSP00000513397.1:n.-207+29_-207+30delinsTG
ENST00000697687.1:n.64_65delinsTG
ENST00000697688.1:n.64_65delinsTG
ENST00000697689.1:c.18_19delinsTG ENSP00000513398.1:p.Arg7Gly
ENST00000697690.1:c.18_19delinsTG ENSP00000513399.1:p.Arg7Gly
ENST00000697691.1:c.18_19delinsTG ENSP00000513400.1:p.Arg7Gly
ENST00000697692.1:c.18_19delinsTG ENSP00000513401.1:p.Arg7Gly
XM_006722001.2:c.18_19delinsTG XP_006722064.1:p.Arg7Gly
XM_006722001.4:c.18_19delinsTG XP_006722064.1:p.Arg7Gly
XM_006722002.2:c.18_19delinsTG XP_006722065.1:p.Arg7Gly
XM_006722002.4:c.18_19delinsTG XP_006722065.1:p.Arg7Gly
XM_006722004.2:c.-231_-230delinsTG XP_006722067.1:n.-231_-230delinsTG
XM_006722004.3:c.-231_-230delinsTG XP_006722067.1:n.-231_-230delinsTG
XM_006722005.2:c.-207+29_-207+30delinsTG XP_006722068.1:n.-207+29_-207+30delinsTG
XM_006722005.3:c.-207+29_-207+30delinsTG XP_006722068.1:n.-207+29_-207+30delinsTG
XM_011525092.1:c.-531_-530delinsTG XP_011523394.1:n.-531_-530delinsTG
XM_011525093.1:c.-692_-691delinsTG XP_011523395.1:n.-692_-691delinsTG
XM_017024914.1:c.-231_-230delinsTG XP_016880403.1:n.-231_-230delinsTG
XM_017024916.1:c.-531_-530delinsTG XP_016880405.1:n.-531_-530delinsTG
XM_017024917.1:c.-207+29_-207+30delinsTG XP_016880406.1:n.-207+29_-207+30delinsTG
XM_017024918.2:c.-505_-504delinsTG XP_016880407.1:n.-505_-504delinsTG
XR_934513.1:n.91_92delinsTG
XR_934513.3:n.522_523delinsTG
XR_934514.1:n.91_92delinsTG
XR_934514.3:n.522_523delinsTG