Canonical Allele Identifier: CA3057243164
Community Standard Title: NM_058216.3(RAD51C):c.957_958delinsTG (p.Lys320Glu)
Gene: RAD51C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58724092_58724093delinsTG , CM000679.2:g.58724092_58724093delinsTG GRCh38
NC_000017.10:g.56801453_56801454delinsTG , CM000679.1:g.56801453_56801454delinsTG GRCh37
NC_000017.9:g.54156452_54156453delinsTG NCBI36
NG_023199.1:g.36491_36492delinsTG , LRG_314:g.36491_36492delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_058216.3:c.957_958delinsTG MANE Select NP_478123.1:p.Lys320Glu
ENST00000337432.9:c.957_958delinsTG MANE Select ENSP00000336701.4:p.Lys320Glu
NM_058216.2:c.957_958delinsTG NP_478123.1:p.Lys320Glu
NR_103872.1:n.861_862delinsTG
NR_103872.2:n.832_833delinsTG
ENST00000337432.8:c.957_958delinsTG ENSP00000336701.4:p.Lys320Glu
ENST00000413590.5:c.595_596delinsTG
ENST00000461271.6:c.606_607delinsTG ENSP00000464056.2:p.Lys203Glu
ENST00000475762.5:c.*1593_*1594delinsTG ENSP00000432421.1:n.*1593_*1594delinsTG
ENST00000482007.5:c.*385_*386delinsTG ENSP00000433332.1:n.*385_*386delinsTG
ENST00000487525.5:c.*530_*531delinsTG ENSP00000431637.1:n.*530_*531delinsTG
ENST00000578151.1:n.239+3280_239+3281delinsTG
ENST00000581221.5:n.472_473delinsTG
ENST00000583539.5:c.957_958delinsTG ENSP00000463121.1:p.Lys320Glu
ENST00000584617.5:c.679_680delinsTG
ENST00000584804.1:c.199+3280_199+3281delinsTG ENSP00000463658.1:n.199+3280_199+3281delinsTG
ENST00000697680.1:c.*1921_*1922delinsTG ENSP00000513392.1:n.*1921_*1922delinsTG
ENST00000697681.1:c.*2118_*2119delinsTG ENSP00000513393.1:n.*2118_*2119delinsTG
ENST00000697683.1:c.*1821_*1822delinsTG ENSP00000513395.1:n.*1821_*1822delinsTG
ENST00000697684.1:n.1017_1018delinsTG
ENST00000697685.1:c.*1654_*1655delinsTG ENSP00000513396.1:n.*1654_*1655delinsTG
ENST00000697686.1:c.606_607delinsTG ENSP00000513397.1:p.Lys203Glu
ENST00000697687.1:n.836_837delinsTG
ENST00000697688.1:n.1003_1004delinsTG
ENST00000697689.1:c.*1440+3280_*1440+3281delinsTG ENSP00000513398.1:n.*1440+3280_*1440+3281delinsTG
ENST00000697690.1:c.904+3280_904+3281delinsTG ENSP00000513399.1:n.904+3280_904+3281delinsTG
ENST00000697691.1:c.*929_*930delinsTG ENSP00000513400.1:n.*929_*930delinsTG
ENST00000697692.1:c.*969_*970delinsTG ENSP00000513401.1:n.*969_*970delinsTG
ENST00000697694.1:c.606_607delinsTG ENSP00000513402.1:p.Lys203Glu
ENST00000697695.1:n.1564_1565delinsTG
XM_006722001.2:c.957_958delinsTG XP_006722064.1:p.Lys320Glu
XM_006722001.4:c.957_958delinsTG XP_006722064.1:p.Lys320Glu
XM_006722002.2:c.904+3280_904+3281delinsTG XP_006722065.1:n.904+3280_904+3281delinsTG
XM_006722002.4:c.904+3280_904+3281delinsTG XP_006722065.1:n.904+3280_904+3281delinsTG
XM_006722004.2:c.606_607delinsTG XP_006722067.1:p.Lys203Glu
XM_006722004.3:c.606_607delinsTG XP_006722067.1:p.Lys203Glu
XM_006722005.2:c.606_607delinsTG XP_006722068.1:p.Lys203Glu
XM_006722005.3:c.606_607delinsTG XP_006722068.1:p.Lys203Glu
XM_011525092.1:c.606_607delinsTG XP_011523394.1:p.Lys203Glu
XM_011525092.2:c.606_607delinsTG XP_011523394.1:p.Lys203Glu
XM_011525093.1:c.606_607delinsTG XP_011523395.1:p.Lys203Glu
XM_011525093.2:c.606_607delinsTG XP_011523395.1:p.Lys203Glu
XM_011525094.1:c.606_607delinsTG XP_011523396.1:p.Lys203Glu
XM_011525094.2:c.606_607delinsTG XP_011523396.1:p.Lys203Glu
XM_017024914.1:c.606_607delinsTG XP_016880403.1:p.Lys203Glu
XM_017024915.1:c.606_607delinsTG XP_016880404.1:p.Lys203Glu
XM_017024916.1:c.606_607delinsTG XP_016880405.1:p.Lys203Glu
XM_017024917.1:c.606_607delinsTG XP_016880406.1:p.Lys203Glu
XM_017024918.2:c.606_607delinsTG XP_016880407.1:p.Lys203Glu
XM_017024919.1:c.553+3280_553+3281delinsTG XP_016880408.1:n.553+3280_553+3281delinsTG
XR_934513.1:n.1175_1176delinsTG
XR_934513.3:n.1606_1607delinsTG
XR_934514.1:n.1175_1176delinsTG
XR_934514.3:n.1606_1607delinsTG