Canonical Allele Identifier: CA2399201784
Gene: HPS4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26457896A= , CM000684.2:g.26457896A= GRCh38
NC_000022.10:g.26853862A= , CM000684.1:g.26853862A= GRCh37
NC_000022.9:g.25183862A= NCBI36
NG_009763.2:g.30968T= , LRG_590:g.30968T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422379.3:c.1972T= ENSP00000415081.3:p.Phe658=
ENST00000473782.2:c.1918T= ENSP00000514223.1:p.Phe640=
ENST00000483631.2:c.1123T= ENSP00000514228.1:p.Phe375=
ENST00000491142.2:c.1918T= ENSP00000514221.1:p.Phe640=
ENST00000699226.1:n.4844T=
ENST00000699227.1:c.*1262T= ENSP00000514220.1:n.*1262T=
ENST00000699228.1:n.2468T=
ENST00000699229.1:n.1335T=
ENST00000699230.1:n.2641T=
ENST00000699231.1:n.4930T=
ENST00000699232.1:n.3274T=
ENST00000699233.1:n.1789T=
ENST00000699234.1:c.*1262T= ENSP00000514222.1:n.*1262T=
ENST00000699235.1:c.1123T= ENSP00000514224.1:p.Phe375=
ENST00000699236.1:c.*1107T= ENSP00000514225.1:n.*1107T=
ENST00000699237.1:c.*1107T= ENSP00000514226.1:n.*1107T=
ENST00000699238.1:c.*1461T= ENSP00000514227.1:n.*1461T=
ENST00000699239.1:n.4672T=
ENST00000699240.1:c.*1575T= ENSP00000514229.1:n.*1575T=
ENST00000699241.1:c.*2110T= ENSP00000514230.1:n.*2110T=
ENST00000699242.1:c.1828T= ENSP00000514231.1:p.Phe610=
ENST00000699243.1:c.*1262T= ENSP00000514232.1:n.*1262T=
ENST00000699244.1:c.1771T= ENSP00000514233.1:p.Phe591=
ENST00000699245.1:n.1210T=
ENST00000699246.1:c.*1289T= ENSP00000514234.1:n.*1289T=
ENST00000699247.1:c.874T= ENSP00000514235.1:p.Phe292=
ENST00000699248.1:n.3784-4492T=
ENST00000699249.1:c.*1058-4492T= ENSP00000514236.1:n.*1058-4492T=
ENST00000699250.1:c.1714-4492T= ENSP00000514237.1:n.1714-4492T=
ENST00000699251.1:c.1918T= ENSP00000514238.1:p.Phe640=
ENST00000699252.1:n.2468T=
ENST00000398145.7:c.1918T= MANE Select ENSP00000381213.2:p.Phe640=
ENST00000336873.9:c.1918T= ENSP00000338457.5:p.Phe640=
ENST00000398145.6:c.1918T= ENSP00000381213.2:p.Phe640=
ENST00000402105.7:c.1903T= ENSP00000384185.3:p.Phe635=
ENST00000429411.5:c.*1490T= ENSP00000399705.1:n.*1490T=
ENST00000439453.5:c.*1436T= ENSP00000406764.1:n.*1436T=
ENST00000464362.5:c.*2249T= ENSP00000430291.1:n.*2249T=
ENST00000466781.5:n.4777T=
ENST00000485842.5:n.609T=
ENST00000493455.6:n.481T=
ENST00000496385.5:n.2480-4492T=
ENST00000519774.5:n.304T=
NM_022081.5:c.1918T= , LRG_590t1:c.1918T= NP_071364.4:p.Phe640=
NM_152841.2:c.1903T= , LRG_590t2:c.1903T= NP_690054.1:p.Phe635=
NR_073135.1:n.2604T=
NR_073136.1:n.2366T=
XM_006724353.2:c.1972T= XP_006724416.1:p.Phe658=
XM_006724354.2:c.1972T= XP_006724417.1:p.Phe658=
XM_006724360.2:c.1405T= XP_006724423.1:p.Phe469=
XM_011530485.1:c.2050T= XP_011528787.1:p.Phe684=
XM_011530486.1:c.2050T= XP_011528788.1:p.Phe684=
XM_011530487.1:c.2050T= XP_011528789.1:p.Phe684=
XM_011530488.1:c.2050T= XP_011528790.1:p.Phe684=
XM_011530489.1:c.2050T= XP_011528791.1:p.Phe684=
XM_011530490.1:c.1996T= XP_011528792.1:p.Phe666=
XM_011530491.1:c.2050T= XP_011528793.1:p.Phe684=
XM_011530492.1:c.2050T= XP_011528794.1:p.Phe684=
XM_011530493.1:c.1846-4492T= XP_011528795.1:n.1846-4492T=
XM_011530494.1:c.1258T= XP_011528796.1:p.Phe420=
XM_011530495.1:c.1405T= XP_011528797.1:p.Phe469=
XM_011530496.1:c.1258T= XP_011528798.1:p.Phe420=
XR_937947.1:n.2709T=
NM_001349896.1:c.1918T= NP_001336825.1:p.Phe640=
NM_001349898.1:c.1918T= NP_001336827.1:p.Phe640=
NM_001349899.1:c.1918T= NP_001336828.1:p.Phe640=
NM_001349900.1:c.1972T= NP_001336829.1:p.Phe658=
NM_001349901.1:c.1972T= NP_001336830.1:p.Phe658=
NM_001349902.1:c.1714-4492T= NP_001336831.1:n.1714-4492T=
NM_001349903.1:c.1714-4492T= NP_001336832.1:n.1714-4492T=
NM_001349904.1:c.1918T= NP_001336833.1:p.Phe640=
NM_001349905.1:c.1918T= NP_001336834.1:p.Phe640=
NR_146311.1:n.2695T=
NR_146312.1:n.2520T=
NR_146313.1:n.2540T=
NR_146314.1:n.2671T=
NR_146315.1:n.2611T=
NR_146316.1:n.2586T=
XM_006724360.3:c.1405T= XP_006724423.1:p.Phe469=
XM_011530485.2:c.2050T= XP_011528787.1:p.Phe684=
XM_011530486.2:c.2050T= XP_011528788.1:p.Phe684=
XM_011530487.2:c.2050T= XP_011528789.1:p.Phe684=
XM_011530488.2:c.2050T= XP_011528790.1:p.Phe684=
XM_011530489.2:c.2050T= XP_011528791.1:p.Phe684=
XM_011530490.3:c.1996T= XP_011528792.1:p.Phe666=
XM_011530491.3:c.2050T= XP_011528793.1:p.Phe684=
XM_011530492.2:c.2050T= XP_011528794.1:p.Phe684=
XM_011530493.3:c.1846-4492T= XP_011528795.1:n.1846-4492T=
XM_011530494.2:c.1258T= XP_011528796.1:p.Phe420=
XM_011530495.2:c.1405T= XP_011528797.1:p.Phe469=
XM_011530496.2:c.1258T= XP_011528798.1:p.Phe420=
XM_017029045.2:c.1996T= XP_016884534.1:p.Phe666=
XM_017029046.2:c.1918T= XP_016884535.1:p.Phe640=
XM_017029047.2:c.1792-4492T= XP_016884536.1:n.1792-4492T=
XM_017029052.2:c.1510T= XP_016884541.1:p.Phe504=
XM_017029053.1:c.1495T= XP_016884542.1:p.Phe499=
XM_017029056.2:c.1123T= XP_016884545.1:p.Phe375=
XM_017029061.2:c.1123T= XP_016884550.1:p.Phe375=
XM_017029062.2:c.1123T= XP_016884551.1:p.Phe375=
XM_017029063.2:c.1123T= XP_016884552.1:p.Phe375=
XM_017029064.2:c.1123T= XP_016884553.1:p.Phe375=
XM_024452298.1:c.1291T= XP_024308066.1:p.Phe431=
XM_024452299.1:c.1123T= XP_024308067.1:p.Phe375=
XM_024452300.1:c.1123T= XP_024308068.1:p.Phe375=
XR_001755361.2:n.2626T=
XR_001755364.1:n.2278-4492T=
XR_001755366.2:n.3155T=
XR_002958721.1:n.2500-4492T=
XR_937947.2:n.2704T=
NM_001349898.2:c.1918T= NP_001336827.1:p.Phe640=
NM_001349899.2:c.1918T= NP_001336828.1:p.Phe640=
NM_001349900.2:c.1972T= NP_001336829.1:p.Phe658=
NM_001349903.2:c.1714-4492T= NP_001336832.1:n.1714-4492T=
NM_001349904.2:c.1918T= NP_001336833.1:p.Phe640=
NR_073136.2:n.2173T=
NR_146311.2:n.2615T=
NR_146313.2:n.2460T=
NR_146315.2:n.2531T=
NM_022081.6:c.1918T= MANE Select NP_071364.4:p.Phe640=
NR_146316.2:n.2506T=