Canonical Allele Identifier: CA1930882825
Gene: HPS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.98430580G= , CM000672.2:g.98430580G= GRCh38
NC_000010.10:g.100190337G= , CM000672.1:g.100190337G= GRCh37
NC_000010.9:g.100180327G= NCBI36
NG_009646.1:g.21368C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000414009.2:c.759C= ENSP00000392462.2:p.Asp253=
ENST00000699112.1:c.498C= ENSP00000514137.1:p.Asp166=
ENST00000699113.1:c.*236C= ENSP00000514138.1:n.*236C=
ENST00000699114.1:n.745C=
ENST00000699115.1:c.759C= ENSP00000514139.1:p.Asp253=
ENST00000699116.1:n.660C=
ENST00000699117.1:n.1510C=
ENST00000699118.1:c.551-3316C= ENSP00000514140.1:n.551-3316C=
ENST00000699119.1:c.*217C= ENSP00000514141.1:n.*217C=
ENST00000699120.1:c.*217C= ENSP00000514142.1:n.*217C=
ENST00000699121.1:c.*217C= ENSP00000514143.1:n.*217C=
ENST00000699122.1:c.365-3316C= ENSP00000514144.1:n.365-3316C=
ENST00000699123.1:c.*527C= ENSP00000514145.1:n.*527C=
ENST00000699124.1:n.849C=
ENST00000699125.1:c.641C= ENSP00000514146.1:p.Thr214=
ENST00000699126.1:n.1002C=
ENST00000699127.1:n.1002C=
ENST00000699128.1:c.759C= ENSP00000514147.1:p.Asp253=
ENST00000699129.1:c.759C= ENSP00000514148.1:p.Asp253=
ENST00000699130.1:n.1002C=
ENST00000699131.1:c.759C= ENSP00000514149.1:p.Asp253=
ENST00000699132.1:n.2225C=
ENST00000699133.1:c.759C= ENSP00000514150.1:p.Asp253=
ENST00000699134.1:c.869C= ENSP00000514151.1:p.Thr290=
ENST00000699135.1:c.*236C= ENSP00000514152.1:n.*236C=
ENST00000699136.1:c.759C= ENSP00000514153.1:p.Asp253=
ENST00000699137.1:c.551-3316C= ENSP00000514154.1:n.551-3316C=
ENST00000699138.1:c.*217C= ENSP00000514155.1:n.*217C=
ENST00000699139.1:c.498C= ENSP00000514156.1:p.Asp166=
ENST00000699140.1:c.759C= ENSP00000514157.1:p.Asp253=
ENST00000699141.1:c.*217C= ENSP00000514158.1:n.*217C=
ENST00000699142.1:c.759C= ENSP00000514159.1:p.Asp253=
ENST00000699143.1:c.*217C= ENSP00000514160.1:n.*217C=
ENST00000699144.1:c.*217C= ENSP00000514161.1:n.*217C=
ENST00000699145.1:c.759C= ENSP00000514162.1:p.Asp253=
ENST00000699146.1:c.759C= ENSP00000514164.1:p.Asp253=
ENST00000699147.1:c.*217C= ENSP00000514165.1:n.*217C=
ENST00000699149.1:n.1002C=
ENST00000699150.1:n.841C=
ENST00000699151.1:n.2225C=
ENST00000699152.1:n.2427C=
ENST00000699153.1:c.*217C= ENSP00000514166.1:n.*217C=
ENST00000699154.1:n.1137C=
ENST00000699159.1:c.*217C= ENSP00000514167.1:n.*217C=
ENST00000361490.9:c.759C= MANE Select ENSP00000355310.4:p.Asp253=
ENST00000325103.10:c.759C= ENSP00000326649.6:p.Asp253=
ENST00000338546.9:c.759C= ENSP00000343638.5:p.Asp253=
ENST00000359632.7:c.243C= ENSP00000352652.3:p.Asp81=
ENST00000361490.8:c.759C= ENSP00000355310.4:p.Asp253=
ENST00000414009.1:c.361C=
ENST00000467246.5:n.997C=
ENST00000470095.5:n.243C=
ENST00000478087.5:n.404C=
ENST00000480020.5:n.786C=
ENST00000498219.5:n.636C=
ENST00000613394.4:c.759C= ENSP00000477926.1:p.Asp253=
NM_000195.3:c.759C= NP_000186.2:p.Asp253=
NM_000195.4:c.759C= NP_000186.2:p.Asp253=
NM_001311345.1:c.-115C= NP_001298274.1:n.-115C=
NM_182639.2:c.759C= NP_872577.1:p.Asp253=
NM_182639.3:c.759C= NP_872577.1:p.Asp253=
XM_005269755.2:c.759C= XP_005269812.1:p.Asp253=
XM_005269756.2:c.759C= XP_005269813.1:p.Asp253=
XM_005269757.3:c.759C= XP_005269814.1:p.Asp253=
XM_005269758.1:c.759C= XP_005269815.1:p.Asp253=
XM_005269759.1:c.390C= XP_005269816.1:p.Asp130=
XM_005269760.3:c.-115C= XP_005269817.1:n.-115C=
XM_005269761.1:c.-115C= XP_005269818.1:n.-115C=
XM_006717818.1:c.498C= XP_006717881.1:p.Asp166=
NM_001322476.1:c.759C= NP_001309405.1:p.Asp253=
NM_001322477.1:c.759C= NP_001309406.1:p.Asp253=
NM_001322478.1:c.759C= NP_001309407.1:p.Asp253=
NM_001322479.1:c.759C= NP_001309408.1:p.Asp253=
NM_001322480.1:c.498C= NP_001309409.1:p.Asp166=
NM_001322481.1:c.498C= NP_001309410.1:p.Asp166=
NM_001322482.1:c.498C= NP_001309411.1:p.Asp166=
NM_001322483.1:c.390C= NP_001309412.1:p.Asp130=
NM_001322484.1:c.390C= NP_001309413.1:p.Asp130=
NM_001322485.1:c.390C= NP_001309414.1:p.Asp130=
NM_001322487.1:c.-214C= NP_001309416.1:n.-214C=
NM_001322489.1:c.-115C= NP_001309418.1:n.-115C=
NM_001322490.1:c.641C= NP_001309419.1:p.Thr214=
NM_001322491.1:c.759C= NP_001309420.1:p.Asp253=
NM_001322492.1:c.641C= NP_001309421.1:p.Thr214=
XM_005269757.4:c.759C= XP_005269814.1:p.Asp253=
XM_017016170.1:c.498C= XP_016871659.1:p.Asp166=
XM_017016171.2:c.390C= XP_016871660.1:p.Asp130=
XM_017016172.2:c.-115C= XP_016871661.1:n.-115C=
XM_017016173.1:c.641C= XP_016871662.1:p.Thr214=
XM_024447971.1:c.641C= XP_024303739.1:p.Thr214=
XM_024447972.1:c.-214C= XP_024303740.1:n.-214C=
XR_001747098.1:n.1028C=
XR_001747099.2:n.1028C=
XR_001747100.2:n.1028C=
XR_001747101.2:n.1028C=
NM_000195.5:c.759C= MANE Select NP_000186.2:p.Asp253=
NM_001311345.2:c.-115C= NP_001298274.1:n.-115C=
NM_001322476.2:c.759C= NP_001309405.1:p.Asp253=
NM_001322477.2:c.759C= NP_001309406.1:p.Asp253=
NM_001322478.2:c.759C= NP_001309407.1:p.Asp253=
NM_001322479.2:c.759C= NP_001309408.1:p.Asp253=
NM_001322480.2:c.498C= NP_001309409.1:p.Asp166=
NM_001322481.2:c.498C= NP_001309410.1:p.Asp166=
NM_001322482.2:c.498C= NP_001309411.1:p.Asp166=
NM_001322483.2:c.390C= NP_001309412.1:p.Asp130=
NM_001322484.2:c.390C= NP_001309413.1:p.Asp130=
NM_001322485.2:c.390C= NP_001309414.1:p.Asp130=
NM_001322487.2:c.-214C= NP_001309416.1:n.-214C=
NM_001322489.2:c.-115C= NP_001309418.1:n.-115C=
NM_001322490.2:c.641C= NP_001309419.1:p.Thr214=
NM_001322491.2:c.759C= NP_001309420.1:p.Asp253=
NM_001322492.2:c.641C= NP_001309421.1:p.Thr214=
NM_182639.4:c.759C= NP_872577.1:p.Asp253=