Canonical Allele Identifier: CA2399201816
Gene: HPS4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.26457946G= , CM000684.2:g.26457946G= GRCh38
NC_000022.10:g.26853912G= , CM000684.1:g.26853912G= GRCh37
NC_000022.9:g.25183912G= NCBI36
NG_009763.2:g.30918C= , LRG_590:g.30918C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000422379.3:c.1922C= ENSP00000415081.3:p.Thr641=
ENST00000473782.2:c.1868C= ENSP00000514223.1:p.Thr623=
ENST00000483631.2:c.1073C= ENSP00000514228.1:p.Thr358=
ENST00000491142.2:c.1868C= ENSP00000514221.1:p.Thr623=
ENST00000699226.1:n.4794C=
ENST00000699227.1:c.*1212C= ENSP00000514220.1:n.*1212C=
ENST00000699228.1:n.2418C=
ENST00000699229.1:n.1285C=
ENST00000699230.1:n.2591C=
ENST00000699231.1:n.4880C=
ENST00000699232.1:n.3224C=
ENST00000699233.1:n.1739C=
ENST00000699234.1:c.*1212C= ENSP00000514222.1:n.*1212C=
ENST00000699235.1:c.1073C= ENSP00000514224.1:p.Thr358=
ENST00000699236.1:c.*1057C= ENSP00000514225.1:n.*1057C=
ENST00000699237.1:c.*1057C= ENSP00000514226.1:n.*1057C=
ENST00000699238.1:c.*1411C= ENSP00000514227.1:n.*1411C=
ENST00000699239.1:n.4622C=
ENST00000699240.1:c.*1525C= ENSP00000514229.1:n.*1525C=
ENST00000699241.1:c.*2060C= ENSP00000514230.1:n.*2060C=
ENST00000699242.1:c.1778C= ENSP00000514231.1:p.Thr593=
ENST00000699243.1:c.*1212C= ENSP00000514232.1:n.*1212C=
ENST00000699244.1:c.1721C= ENSP00000514233.1:p.Thr574=
ENST00000699245.1:n.1160C=
ENST00000699246.1:c.*1239C= ENSP00000514234.1:n.*1239C=
ENST00000699247.1:c.824C= ENSP00000514235.1:p.Thr275=
ENST00000699248.1:n.3784-4542C=
ENST00000699249.1:c.*1058-4542C= ENSP00000514236.1:n.*1058-4542C=
ENST00000699250.1:c.1714-4542C= ENSP00000514237.1:n.1714-4542C=
ENST00000699251.1:c.1868C= ENSP00000514238.1:p.Thr623=
ENST00000699252.1:n.2418C=
ENST00000398145.7:c.1868C= MANE Select ENSP00000381213.2:p.Thr623=
ENST00000336873.9:c.1868C= ENSP00000338457.5:p.Thr623=
ENST00000398145.6:c.1868C= ENSP00000381213.2:p.Thr623=
ENST00000402105.7:c.1853C= ENSP00000384185.3:p.Thr618=
ENST00000429411.5:c.*1440C= ENSP00000399705.1:n.*1440C=
ENST00000439453.5:c.*1386C= ENSP00000406764.1:n.*1386C=
ENST00000464362.5:c.*2199C= ENSP00000430291.1:n.*2199C=
ENST00000466781.5:n.4727C=
ENST00000485842.5:n.559C=
ENST00000493455.6:n.431C=
ENST00000496385.5:n.2480-4542C=
ENST00000519774.5:n.254C=
NM_022081.5:c.1868C= , LRG_590t1:c.1868C= NP_071364.4:p.Thr623=
NM_152841.2:c.1853C= , LRG_590t2:c.1853C= NP_690054.1:p.Thr618=
NR_073135.1:n.2554C=
NR_073136.1:n.2316C=
XM_006724353.2:c.1922C= XP_006724416.1:p.Thr641=
XM_006724354.2:c.1922C= XP_006724417.1:p.Thr641=
XM_006724360.2:c.1355C= XP_006724423.1:p.Thr452=
XM_011530485.1:c.2000C= XP_011528787.1:p.Thr667=
XM_011530486.1:c.2000C= XP_011528788.1:p.Thr667=
XM_011530487.1:c.2000C= XP_011528789.1:p.Thr667=
XM_011530488.1:c.2000C= XP_011528790.1:p.Thr667=
XM_011530489.1:c.2000C= XP_011528791.1:p.Thr667=
XM_011530490.1:c.1946C= XP_011528792.1:p.Thr649=
XM_011530491.1:c.2000C= XP_011528793.1:p.Thr667=
XM_011530492.1:c.2000C= XP_011528794.1:p.Thr667=
XM_011530493.1:c.1846-4542C= XP_011528795.1:n.1846-4542C=
XM_011530494.1:c.1208C= XP_011528796.1:p.Thr403=
XM_011530495.1:c.1355C= XP_011528797.1:p.Thr452=
XM_011530496.1:c.1208C= XP_011528798.1:p.Thr403=
XR_937947.1:n.2659C=
NM_001349896.1:c.1868C= NP_001336825.1:p.Thr623=
NM_001349898.1:c.1868C= NP_001336827.1:p.Thr623=
NM_001349899.1:c.1868C= NP_001336828.1:p.Thr623=
NM_001349900.1:c.1922C= NP_001336829.1:p.Thr641=
NM_001349901.1:c.1922C= NP_001336830.1:p.Thr641=
NM_001349902.1:c.1714-4542C= NP_001336831.1:n.1714-4542C=
NM_001349903.1:c.1714-4542C= NP_001336832.1:n.1714-4542C=
NM_001349904.1:c.1868C= NP_001336833.1:p.Thr623=
NM_001349905.1:c.1868C= NP_001336834.1:p.Thr623=
NR_146311.1:n.2645C=
NR_146312.1:n.2470C=
NR_146313.1:n.2490C=
NR_146314.1:n.2621C=
NR_146315.1:n.2561C=
NR_146316.1:n.2536C=
XM_006724360.3:c.1355C= XP_006724423.1:p.Thr452=
XM_011530485.2:c.2000C= XP_011528787.1:p.Thr667=
XM_011530486.2:c.2000C= XP_011528788.1:p.Thr667=
XM_011530487.2:c.2000C= XP_011528789.1:p.Thr667=
XM_011530488.2:c.2000C= XP_011528790.1:p.Thr667=
XM_011530489.2:c.2000C= XP_011528791.1:p.Thr667=
XM_011530490.3:c.1946C= XP_011528792.1:p.Thr649=
XM_011530491.3:c.2000C= XP_011528793.1:p.Thr667=
XM_011530492.2:c.2000C= XP_011528794.1:p.Thr667=
XM_011530493.3:c.1846-4542C= XP_011528795.1:n.1846-4542C=
XM_011530494.2:c.1208C= XP_011528796.1:p.Thr403=
XM_011530495.2:c.1355C= XP_011528797.1:p.Thr452=
XM_011530496.2:c.1208C= XP_011528798.1:p.Thr403=
XM_017029045.2:c.1946C= XP_016884534.1:p.Thr649=
XM_017029046.2:c.1868C= XP_016884535.1:p.Thr623=
XM_017029047.2:c.1792-4542C= XP_016884536.1:n.1792-4542C=
XM_017029052.2:c.1460C= XP_016884541.1:p.Thr487=
XM_017029053.1:c.1445C= XP_016884542.1:p.Thr482=
XM_017029056.2:c.1073C= XP_016884545.1:p.Thr358=
XM_017029061.2:c.1073C= XP_016884550.1:p.Thr358=
XM_017029062.2:c.1073C= XP_016884551.1:p.Thr358=
XM_017029063.2:c.1073C= XP_016884552.1:p.Thr358=
XM_017029064.2:c.1073C= XP_016884553.1:p.Thr358=
XM_024452298.1:c.1241C= XP_024308066.1:p.Thr414=
XM_024452299.1:c.1073C= XP_024308067.1:p.Thr358=
XM_024452300.1:c.1073C= XP_024308068.1:p.Thr358=
XR_001755361.2:n.2576C=
XR_001755364.1:n.2278-4542C=
XR_001755366.2:n.3105C=
XR_002958721.1:n.2500-4542C=
XR_937947.2:n.2654C=
NM_001349898.2:c.1868C= NP_001336827.1:p.Thr623=
NM_001349899.2:c.1868C= NP_001336828.1:p.Thr623=
NM_001349900.2:c.1922C= NP_001336829.1:p.Thr641=
NM_001349903.2:c.1714-4542C= NP_001336832.1:n.1714-4542C=
NM_001349904.2:c.1868C= NP_001336833.1:p.Thr623=
NR_073136.2:n.2123C=
NR_146311.2:n.2565C=
NR_146313.2:n.2410C=
NR_146315.2:n.2481C=
NM_022081.6:c.1868C= MANE Select NP_071364.4:p.Thr623=
NR_146316.2:n.2456C=