Canonical Allele Identifier: CA341619
Gene: HPS1 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.98425689del , CM000672.2:g.98425689del GRCh38
NC_000010.10:g.100185446del , CM000672.1:g.100185446del GRCh37
NC_000010.9:g.100175436del NCBI36
NG_009646.1:g.26261del

Transcript Alleles

HGVS Amino-acid Change
ENST00000699112.1:c.829del ENSP00000514137.1:p.Gln277SerfsTer2
ENST00000699113.1:c.*567del ENSP00000514138.1:n.*567del
ENST00000699114.1:n.1076del
ENST00000699115.1:c.922del ENSP00000514139.1:p.Gln308SerfsTer2
ENST00000699116.1:n.3148del
ENST00000699117.1:n.1841del
ENST00000699118.1:c.802del ENSP00000514140.1:p.Gln268SerfsTer2
ENST00000699119.1:c.*380del ENSP00000514141.1:n.*380del
ENST00000699120.1:c.*647del ENSP00000514142.1:n.*647del
ENST00000699121.1:c.*548del ENSP00000514143.1:n.*548del
ENST00000699122.1:c.616del ENSP00000514144.1:p.Gln206SerfsTer2
ENST00000699123.1:c.*957del ENSP00000514145.1:n.*957del
ENST00000699124.1:n.2508del
ENST00000699125.1:c.1219del ENSP00000514146.1:p.Gln407SerfsTer2
ENST00000699126.1:n.2661del
ENST00000699127.1:n.1432del
ENST00000699128.1:c.*328del ENSP00000514147.1:n.*328del
ENST00000699129.1:c.*328del ENSP00000514148.1:n.*328del
ENST00000699130.1:n.2562del
ENST00000699131.1:c.1021del ENSP00000514149.1:p.Gln341SerfsTer2
ENST00000699132.1:n.3484del
ENST00000699133.1:c.922del ENSP00000514150.1:p.Gln308SerfsTer2
ENST00000699134.1:c.1447del ENSP00000514151.1:p.Gln483SerfsTer2
ENST00000699135.1:c.*399del ENSP00000514152.1:n.*399del
ENST00000699136.1:c.1090del ENSP00000514153.1:p.Gln364SerfsTer2
ENST00000699137.1:c.802del ENSP00000514154.1:p.Gln268SerfsTer2
ENST00000699138.1:c.*647del ENSP00000514155.1:n.*647del
ENST00000699139.1:c.928del ENSP00000514156.1:p.Gln310SerfsTer2
ENST00000699140.1:c.1090del ENSP00000514157.1:p.Gln364SerfsTer2
ENST00000699141.1:c.*647del ENSP00000514158.1:n.*647del
ENST00000699142.1:c.1189del ENSP00000514159.1:p.Gln397SerfsTer2
ENST00000699143.1:c.*548del ENSP00000514160.1:n.*548del
ENST00000699144.1:c.*647del ENSP00000514161.1:n.*647del
ENST00000699145.1:c.1189del ENSP00000514162.1:p.Gln397SerfsTer2
ENST00000699146.1:c.1189del ENSP00000514164.1:p.Gln397SerfsTer2
ENST00000699147.1:c.*647del ENSP00000514165.1:n.*647del
ENST00000699149.1:n.2661del
ENST00000699159.1:c.*548del ENSP00000514167.1:n.*548del
ENST00000361490.9:c.1189del MANE Select ENSP00000355310.4:p.Gln397SerfsTer2
ENST00000325103.10:c.1189del ENSP00000326649.6:p.Gln397SerfsTer2
ENST00000359632.7:c.574del ENSP00000352652.3:p.Gln192SerfsTer2
ENST00000361490.8:c.1189del ENSP00000355310.4:p.Gln397SerfsTer2
ENST00000467246.5:n.1328del
ENST00000470095.5:n.406del
ENST00000478087.5:n.567del
ENST00000497527.1:n.320del
ENST00000613394.4:c.1189del ENSP00000477926.1:p.Gln397SerfsTer2
NM_000195.3:c.1189del NP_000186.2:p.Gln397SerfsTer2
NM_000195.4:c.1189del NP_000186.2:p.Gln397SerfsTer2
NM_001311345.1:c.217del NP_001298274.1:p.Gln73SerfsTer2
XM_005269755.2:c.1189del XP_005269812.1:p.Gln397SerfsTer2
XM_005269756.2:c.1189del XP_005269813.1:p.Gln397SerfsTer2
XM_005269757.3:c.1189del XP_005269814.1:p.Gln397SerfsTer2
XM_005269758.1:c.1090del XP_005269815.1:p.Gln364SerfsTer2
XM_005269759.1:c.820del XP_005269816.1:p.Gln274SerfsTer2
XM_005269760.3:c.217del XP_005269817.1:p.Gln73SerfsTer2
XM_005269761.1:c.217del XP_005269818.1:p.Gln73SerfsTer2
XM_006717818.1:c.928del XP_006717881.1:p.Gln310SerfsTer2
NM_001322476.1:c.1189del NP_001309405.1:p.Gln397SerfsTer2
NM_001322477.1:c.1189del NP_001309406.1:p.Gln397SerfsTer2
NM_001322478.1:c.1090del NP_001309407.1:p.Gln364SerfsTer2
NM_001322479.1:c.1090del NP_001309408.1:p.Gln364SerfsTer2
NM_001322480.1:c.928del NP_001309409.1:p.Gln310SerfsTer2
NM_001322481.1:c.928del NP_001309410.1:p.Gln310SerfsTer2
NM_001322482.1:c.829del NP_001309411.1:p.Gln277SerfsTer2
NM_001322483.1:c.820del NP_001309412.1:p.Gln274SerfsTer2
NM_001322484.1:c.820del NP_001309413.1:p.Gln274SerfsTer2
NM_001322485.1:c.721del NP_001309414.1:p.Gln241SerfsTer2
NM_001322487.1:c.217del NP_001309416.1:p.Gln73SerfsTer2
NM_001322489.1:c.217del NP_001309418.1:p.Gln73SerfsTer2
XM_005269757.4:c.1189del XP_005269814.1:p.Gln397SerfsTer2
XM_017016170.1:c.829del XP_016871659.1:p.Gln277SerfsTer2
XM_017016171.2:c.721del XP_016871660.1:p.Gln241SerfsTer2
XM_017016172.2:c.217del XP_016871661.1:p.Gln73SerfsTer2
XM_024447971.1:c.1219del XP_024303739.1:p.Gln407SerfsTer2
XM_024447972.1:c.217del XP_024303740.1:p.Gln73SerfsTer2
XR_001747098.1:n.1458del
XR_001747099.2:n.1458del
XR_001747100.2:n.1458del
XR_001747101.2:n.1359del
NM_000195.5:c.1189del MANE Select NP_000186.2:p.Gln397SerfsTer2
NM_001311345.2:c.217del NP_001298274.1:p.Gln73SerfsTer2
NM_001322476.2:c.1189del NP_001309405.1:p.Gln397SerfsTer2
NM_001322477.2:c.1189del NP_001309406.1:p.Gln397SerfsTer2
NM_001322478.2:c.1090del NP_001309407.1:p.Gln364SerfsTer2
NM_001322479.2:c.1090del NP_001309408.1:p.Gln364SerfsTer2
NM_001322480.2:c.928del NP_001309409.1:p.Gln310SerfsTer2
NM_001322481.2:c.928del NP_001309410.1:p.Gln310SerfsTer2
NM_001322482.2:c.829del NP_001309411.1:p.Gln277SerfsTer2
NM_001322483.2:c.820del NP_001309412.1:p.Gln274SerfsTer2
NM_001322484.2:c.820del NP_001309413.1:p.Gln274SerfsTer2
NM_001322485.2:c.721del NP_001309414.1:p.Gln241SerfsTer2
NM_001322487.2:c.217del NP_001309416.1:p.Gln73SerfsTer2
NM_001322489.2:c.217del NP_001309418.1:p.Gln73SerfsTer2