Canonical Allele Identifier: CA3260661278
Community Standard Title: NM_001382.4(DPAGT1):c.1176_1177delinsTG (p.Ile393Val)
Gene: DPAGT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119097048_119097049delinsCA , CM000673.2:g.119097048_119097049delinsCA GRCh38
NC_000011.9:g.118967758_118967759delinsCA , CM000673.1:g.118967758_118967759delinsCA GRCh37
NC_000011.8:g.118472968_118472969delinsCA NCBI36
NG_008918.1:g.10027_10028delinsTG

Transcript Alleles

HGVS Amino-acid Change
NM_001382.4:c.1176_1177delinsTG MANE Select NP_001373.2:p.Ile393Val
ENST00000354202.9:c.1176_1177delinsTG MANE Select ENSP00000346142.4:p.Ile393Val
NM_001382.3:c.1176_1177delinsTG NP_001373.2:p.Ile393Val
ENST00000354202.8:c.1176_1177delinsTG ENSP00000346142.4:p.Ile393Val
ENST00000392834.7:c.*881_*882delinsTG ENSP00000376579.3:n.*881_*882delinsTG
ENST00000409993.6:c.1176_1177delinsTG ENSP00000386597.2:p.Ile393Val
ENST00000414373.5:c.*645_*646delinsTG ENSP00000402019.1:n.*645_*646delinsTG
ENST00000442480.1:c.908_909delinsTG ENSP00000406591.1:n.908_909delinsTG
ENST00000445653.6:n.1400_1401delinsTG
ENST00000461999.1:n.1587_1588delinsTG
ENST00000481084.5:n.1805_1806delinsTG
ENST00000524658.2:n.1459_1460delinsTG
ENST00000530052.2:n.2465_2466delinsTG
ENST00000636404.1:c.247_248delinsTG
ENST00000638850.1:c.699_700delinsTG
ENST00000639704.1:c.1083_1084delinsTG ENSP00000491336.1:p.Ile362Val
ENST00000640747.1:c.*851_*852delinsTG ENSP00000492730.1:n.*851_*852delinsTG
ENST00000682191.1:n.1759_1760delinsTG
ENST00000682192.1:n.1622_1623delinsTG
ENST00000682232.1:c.*793_*794delinsTG ENSP00000507302.1:n.*793_*794delinsTG
ENST00000682326.1:c.*146_*147delinsTG ENSP00000508129.1:n.*146_*147delinsTG
ENST00000682404.1:n.2521_2522delinsTG
ENST00000682517.1:n.2746_2747delinsTG
ENST00000682652.1:n.2528_2529delinsTG
ENST00000682665.1:n.2120_2121delinsTG
ENST00000682691.1:n.2042_2043delinsTG
ENST00000682791.1:c.1089_1090delinsTG ENSP00000507312.1:p.Ile364Val
ENST00000682811.1:c.*227_*228delinsTG ENSP00000508196.1:n.*227_*228delinsTG
ENST00000682883.1:n.1280_1281delinsTG
ENST00000682946.1:c.*258_*259delinsTG ENSP00000506856.1:n.*258_*259delinsTG
ENST00000683143.1:c.*881_*882delinsTG ENSP00000507168.1:n.*881_*882delinsTG
ENST00000683373.1:n.1681_1682delinsTG
ENST00000683558.1:n.1925_1926delinsTG
ENST00000683567.1:n.1285_1286delinsTG
ENST00000683955.1:n.1932_1933delinsTG
ENST00000684142.1:c.*1017_*1018delinsTG ENSP00000508008.1:n.*1017_*1018delinsTG
ENST00000684252.1:n.1817_1818delinsTG
ENST00000684255.1:c.*1047_*1048delinsTG ENSP00000507398.1:n.*1047_*1048delinsTG
ENST00000684315.1:n.1987_1988delinsTG
ENST00000684345.1:c.*1320_*1321delinsTG ENSP00000507163.1:n.*1320_*1321delinsTG
ENST00000684499.1:c.*1447_*1448delinsTG ENSP00000506800.1:n.*1447_*1448delinsTG
ENST00000684682.1:c.*1151_*1152delinsTG ENSP00000507326.1:n.*1151_*1152delinsTG
XM_005271422.2:c.1254_1255delinsTG XP_005271479.1:p.Ile419Val
XM_005271422.3:c.1254_1255delinsTG XP_005271479.1:p.Ile419Val
XM_011542648.1:c.933_934delinsTG XP_011540950.1:p.Ile312Val
XM_011542648.2:c.933_934delinsTG XP_011540950.1:p.Ile312Val
XM_017017293.2:c.855_856delinsTG XP_016872782.1:p.Ile286Val
XM_017017294.2:c.*502_*503delinsTG XP_016872783.1:n.*502_*503delinsTG
XM_017017295.1:c.660_661delinsTG XP_016872784.1:p.Ile221Val
XR_001747785.2:n.1210_1211delinsTG
XR_947801.1:n.1335_1336delinsTG
XR_947801.2:n.1122_1123delinsTG