Canonical Allele Identifier: CA378051893

Gene: HPS1

Linked Data

• gnomAD v4: 10-98430579-C-A
• MyVariant Identifiers: chr10:g.100190336C>A (hg19) ; chr10:g.98430579C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.98430579C>A , CM000672.2:g.98430579C>A	GRCh38
NC_000010.10:g.100190336C>A , CM000672.1:g.100190336C>A	GRCh37
NC_000010.9:g.100180326C>A	NCBI36
NG_009646.1:g.21369G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000414009.2:c.760G>T	ENSP00000392462.2:p.Asp254Tyr
ENST00000699112.1:c.499G>T	ENSP00000514137.1:p.Asp167Tyr
ENST00000699113.1:c.*237G>T	ENSP00000514138.1:n.*237G>T
ENST00000699114.1:n.746G>T
ENST00000699115.1:c.760G>T	ENSP00000514139.1:p.Asp254Tyr
ENST00000699116.1:n.661G>T
ENST00000699117.1:n.1511G>T
ENST00000699118.1:c.551-3315G>T	ENSP00000514140.1:n.551-3315G>T
ENST00000699119.1:c.*218G>T	ENSP00000514141.1:n.*218G>T
ENST00000699120.1:c.*218G>T	ENSP00000514142.1:n.*218G>T
ENST00000699121.1:c.*218G>T	ENSP00000514143.1:n.*218G>T
ENST00000699122.1:c.365-3315G>T	ENSP00000514144.1:n.365-3315G>T
ENST00000699123.1:c.*528G>T	ENSP00000514145.1:n.*528G>T
ENST00000699124.1:n.850G>T
ENST00000699125.1:c.642G>T	ENSP00000514146.1:p.Thr214=
ENST00000699126.1:n.1003G>T
ENST00000699127.1:n.1003G>T
ENST00000699128.1:c.760G>T	ENSP00000514147.1:p.Asp254Tyr
ENST00000699129.1:c.760G>T	ENSP00000514148.1:p.Asp254Tyr
ENST00000699130.1:n.1003G>T
ENST00000699131.1:c.760G>T	ENSP00000514149.1:p.Asp254Tyr
ENST00000699132.1:n.2226G>T
ENST00000699133.1:c.760G>T	ENSP00000514150.1:p.Asp254Tyr
ENST00000699134.1:c.870G>T	ENSP00000514151.1:p.Thr290=
ENST00000699135.1:c.*237G>T	ENSP00000514152.1:n.*237G>T
ENST00000699136.1:c.760G>T	ENSP00000514153.1:p.Asp254Tyr
ENST00000699137.1:c.551-3315G>T	ENSP00000514154.1:n.551-3315G>T
ENST00000699138.1:c.*218G>T	ENSP00000514155.1:n.*218G>T
ENST00000699139.1:c.499G>T	ENSP00000514156.1:p.Asp167Tyr
ENST00000699140.1:c.760G>T	ENSP00000514157.1:p.Asp254Tyr
ENST00000699141.1:c.*218G>T	ENSP00000514158.1:n.*218G>T
ENST00000699142.1:c.760G>T	ENSP00000514159.1:p.Asp254Tyr
ENST00000699143.1:c.*218G>T	ENSP00000514160.1:n.*218G>T
ENST00000699144.1:c.*218G>T	ENSP00000514161.1:n.*218G>T
ENST00000699145.1:c.760G>T	ENSP00000514162.1:p.Asp254Tyr
ENST00000699146.1:c.760G>T	ENSP00000514164.1:p.Asp254Tyr
ENST00000699147.1:c.*218G>T	ENSP00000514165.1:n.*218G>T
ENST00000699149.1:n.1003G>T
ENST00000699150.1:n.842G>T
ENST00000699151.1:n.2226G>T
ENST00000699152.1:n.2428G>T
ENST00000699153.1:c.*218G>T	ENSP00000514166.1:n.*218G>T
ENST00000699154.1:n.1138G>T
ENST00000699159.1:c.*218G>T	ENSP00000514167.1:n.*218G>T
ENST00000361490.9:c.760G>T MANE Select	ENSP00000355310.4:p.Asp254Tyr
ENST00000325103.10:c.760G>T	ENSP00000326649.6:p.Asp254Tyr
ENST00000338546.9:c.760G>T	ENSP00000343638.5:p.Asp254Tyr
ENST00000359632.7:c.244G>T	ENSP00000352652.3:p.Asp82Tyr
ENST00000361490.8:c.760G>T	ENSP00000355310.4:p.Asp254Tyr
ENST00000414009.1:c.362G>T
ENST00000467246.5:n.998G>T
ENST00000470095.5:n.244G>T
ENST00000478087.5:n.405G>T
ENST00000480020.5:n.787G>T
ENST00000498219.5:n.637G>T
ENST00000613394.4:c.760G>T	ENSP00000477926.1:p.Asp254Tyr
NM_000195.3:c.760G>T	NP_000186.2:p.Asp254Tyr
NM_000195.4:c.760G>T	NP_000186.2:p.Asp254Tyr
NM_001311345.1:c.-114G>T	NP_001298274.1:n.-114G>T
NM_182639.2:c.760G>T	NP_872577.1:p.Asp254Tyr
NM_182639.3:c.760G>T	NP_872577.1:p.Asp254Tyr
XM_005269755.2:c.760G>T	XP_005269812.1:p.Asp254Tyr
XM_005269756.2:c.760G>T	XP_005269813.1:p.Asp254Tyr
XM_005269757.3:c.760G>T	XP_005269814.1:p.Asp254Tyr
XM_005269758.1:c.760G>T	XP_005269815.1:p.Asp254Tyr
XM_005269759.1:c.391G>T	XP_005269816.1:p.Asp131Tyr
XM_005269760.3:c.-114G>T	XP_005269817.1:n.-114G>T
XM_005269761.1:c.-114G>T	XP_005269818.1:n.-114G>T
XM_006717818.1:c.499G>T	XP_006717881.1:p.Asp167Tyr
NM_001322476.1:c.760G>T	NP_001309405.1:p.Asp254Tyr
NM_001322477.1:c.760G>T	NP_001309406.1:p.Asp254Tyr
NM_001322478.1:c.760G>T	NP_001309407.1:p.Asp254Tyr
NM_001322479.1:c.760G>T	NP_001309408.1:p.Asp254Tyr
NM_001322480.1:c.499G>T	NP_001309409.1:p.Asp167Tyr
NM_001322481.1:c.499G>T	NP_001309410.1:p.Asp167Tyr
NM_001322482.1:c.499G>T	NP_001309411.1:p.Asp167Tyr
NM_001322483.1:c.391G>T	NP_001309412.1:p.Asp131Tyr
NM_001322484.1:c.391G>T	NP_001309413.1:p.Asp131Tyr
NM_001322485.1:c.391G>T	NP_001309414.1:p.Asp131Tyr
NM_001322487.1:c.-213G>T	NP_001309416.1:n.-213G>T
NM_001322489.1:c.-114G>T	NP_001309418.1:n.-114G>T
NM_001322490.1:c.642G>T	NP_001309419.1:p.Thr214=
NM_001322491.1:c.760G>T	NP_001309420.1:p.Asp254Tyr
NM_001322492.1:c.642G>T	NP_001309421.1:p.Thr214=
XM_005269757.4:c.760G>T	XP_005269814.1:p.Asp254Tyr
XM_017016170.1:c.499G>T	XP_016871659.1:p.Asp167Tyr
XM_017016171.2:c.391G>T	XP_016871660.1:p.Asp131Tyr
XM_017016172.2:c.-114G>T	XP_016871661.1:n.-114G>T
XM_017016173.1:c.642G>T	XP_016871662.1:p.Thr214=
XM_024447971.1:c.642G>T	XP_024303739.1:p.Thr214=
XM_024447972.1:c.-213G>T	XP_024303740.1:n.-213G>T
XR_001747098.1:n.1029G>T
XR_001747099.2:n.1029G>T
XR_001747100.2:n.1029G>T
XR_001747101.2:n.1029G>T
NM_000195.5:c.760G>T MANE Select	NP_000186.2:p.Asp254Tyr
NM_001311345.2:c.-114G>T	NP_001298274.1:n.-114G>T
NM_001322476.2:c.760G>T	NP_001309405.1:p.Asp254Tyr
NM_001322477.2:c.760G>T	NP_001309406.1:p.Asp254Tyr
NM_001322478.2:c.760G>T	NP_001309407.1:p.Asp254Tyr
NM_001322479.2:c.760G>T	NP_001309408.1:p.Asp254Tyr
NM_001322480.2:c.499G>T	NP_001309409.1:p.Asp167Tyr
NM_001322481.2:c.499G>T	NP_001309410.1:p.Asp167Tyr
NM_001322482.2:c.499G>T	NP_001309411.1:p.Asp167Tyr
NM_001322483.2:c.391G>T	NP_001309412.1:p.Asp131Tyr
NM_001322484.2:c.391G>T	NP_001309413.1:p.Asp131Tyr
NM_001322485.2:c.391G>T	NP_001309414.1:p.Asp131Tyr
NM_001322487.2:c.-213G>T	NP_001309416.1:n.-213G>T
NM_001322489.2:c.-114G>T	NP_001309418.1:n.-114G>T
NM_001322490.2:c.642G>T	NP_001309419.1:p.Thr214=
NM_001322491.2:c.760G>T	NP_001309420.1:p.Asp254Tyr
NM_001322492.2:c.642G>T	NP_001309421.1:p.Thr214=
NM_182639.4:c.760G>T	NP_872577.1:p.Asp254Tyr