Canonical Allele Identifier: CA10163273

Gene: HPS4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26463989G>A , CM000684.2:g.26463989G>A	GRCh38
NC_000022.10:g.26859955G>A , CM000684.1:g.26859955G>A	GRCh37
NC_000022.9:g.25189955G>A	NCBI36
NG_009763.2:g.24875C>T , LRG_590:g.24875C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022081.6:c.1641C>T MANE Select	NP_071364.4:p.Cys547=
ENST00000398145.7:c.1641C>T MANE Select	ENSP00000381213.2:p.Cys547=
NM_001349896.1:c.1641C>T	NP_001336825.1:p.Cys547=
NM_001349898.1:c.1641C>T	NP_001336827.1:p.Cys547=
NM_001349898.2:c.1641C>T	NP_001336827.1:p.Cys547=
NM_001349899.1:c.1641C>T	NP_001336828.1:p.Cys547=
NM_001349899.2:c.1641C>T	NP_001336828.1:p.Cys547=
NM_001349900.1:c.1695C>T	NP_001336829.1:p.Cys565=
NM_001349900.2:c.1695C>T	NP_001336829.1:p.Cys565=
NM_001349901.1:c.1695C>T	NP_001336830.1:p.Cys565=
NM_001349902.1:c.1641C>T	NP_001336831.1:p.Cys547=
NM_001349903.1:c.1641C>T	NP_001336832.1:p.Cys547=
NM_001349903.2:c.1641C>T	NP_001336832.1:p.Cys547=
NM_001349904.1:c.1641C>T	NP_001336833.1:p.Cys547=
NM_001349904.2:c.1641C>T	NP_001336833.1:p.Cys547=
NM_001349905.1:c.1641C>T	NP_001336834.1:p.Cys547=
NM_022081.5:c.1641C>T , LRG_590t1:c.1641C>T	NP_071364.4:p.Cys547=
NM_152841.2:c.1626C>T , LRG_590t2:c.1626C>T	NP_690054.1:p.Cys542=
NR_073135.1:n.2327C>T
NR_073136.1:n.2089C>T
NR_073136.2:n.1896C>T
NR_146311.1:n.2418C>T
NR_146311.2:n.2338C>T
NR_146312.1:n.2243C>T
NR_146313.1:n.2263C>T
NR_146313.2:n.2183C>T
NR_146314.1:n.2394C>T
NR_146315.1:n.2334C>T
NR_146315.2:n.2254C>T
NR_146316.1:n.2309C>T
NR_146316.2:n.2229C>T
ENST00000336873.9:c.1641C>T	ENSP00000338457.5:p.Cys547=
ENST00000398145.6:c.1641C>T	ENSP00000381213.2:p.Cys547=
ENST00000402105.7:c.1626C>T	ENSP00000384185.3:p.Cys542=
ENST00000422379.3:c.1695C>T	ENSP00000415081.3:p.Cys565=
ENST00000429411.5:c.*1213C>T	ENSP00000399705.1:n.*1213C>T
ENST00000439453.5:c.*1159C>T	ENSP00000406764.1:n.*1159C>T
ENST00000464362.5:c.*1972C>T	ENSP00000430291.1:n.*1972C>T
ENST00000466781.5:n.4500C>T
ENST00000473782.2:c.1641C>T	ENSP00000514223.1:p.Cys547=
ENST00000483631.2:c.846C>T	ENSP00000514228.1:p.Cys282=
ENST00000485842.5:n.404+4562C>T
ENST00000491142.2:c.1641C>T	ENSP00000514221.1:p.Cys547=
ENST00000493455.6:n.204C>T
ENST00000496385.5:n.2407C>T
ENST00000519774.5:n.27C>T
ENST00000699226.1:n.4567C>T
ENST00000699227.1:c.*985C>T	ENSP00000514220.1:n.*985C>T
ENST00000699228.1:n.2191C>T
ENST00000699229.1:n.1058C>T
ENST00000699230.1:n.2364C>T
ENST00000699231.1:n.4653C>T
ENST00000699232.1:n.2997C>T
ENST00000699233.1:n.1512C>T
ENST00000699234.1:c.*985C>T	ENSP00000514222.1:n.*985C>T
ENST00000699235.1:c.846C>T	ENSP00000514224.1:p.Cys282=
ENST00000699236.1:c.*830C>T	ENSP00000514225.1:n.*830C>T
ENST00000699237.1:c.*830C>T	ENSP00000514226.1:n.*830C>T
ENST00000699238.1:c.*1184C>T	ENSP00000514227.1:n.*1184C>T
ENST00000699239.1:n.4395C>T
ENST00000699240.1:c.*1298C>T	ENSP00000514229.1:n.*1298C>T
ENST00000699241.1:c.*1833C>T	ENSP00000514230.1:n.*1833C>T
ENST00000699242.1:c.1551C>T	ENSP00000514231.1:p.Cys517=
ENST00000699243.1:c.*985C>T	ENSP00000514232.1:n.*985C>T
ENST00000699244.1:c.1494C>T	ENSP00000514233.1:p.Cys498=
ENST00000699246.1:c.*1012C>T	ENSP00000514234.1:n.*1012C>T
ENST00000699247.1:c.669+4562C>T	ENSP00000514235.1:n.669+4562C>T
ENST00000699248.1:n.3711C>T
ENST00000699249.1:c.*985C>T	ENSP00000514236.1:n.*985C>T
ENST00000699250.1:c.1641C>T	ENSP00000514237.1:p.Cys547=
ENST00000699251.1:c.1641C>T	ENSP00000514238.1:p.Cys547=
ENST00000699252.1:n.2191C>T
XM_006724353.2:c.1695C>T	XP_006724416.1:p.Cys565=
XM_006724354.2:c.1695C>T	XP_006724417.1:p.Cys565=
XM_006724360.2:c.1128C>T	XP_006724423.1:p.Cys376=
XM_006724360.3:c.1128C>T	XP_006724423.1:p.Cys376=
XM_011530485.1:c.1773C>T	XP_011528787.1:p.Cys591=
XM_011530485.2:c.1773C>T	XP_011528787.1:p.Cys591=
XM_011530486.1:c.1773C>T	XP_011528788.1:p.Cys591=
XM_011530486.2:c.1773C>T	XP_011528788.1:p.Cys591=
XM_011530487.1:c.1773C>T	XP_011528789.1:p.Cys591=
XM_011530487.2:c.1773C>T	XP_011528789.1:p.Cys591=
XM_011530488.1:c.1773C>T	XP_011528790.1:p.Cys591=
XM_011530488.2:c.1773C>T	XP_011528790.1:p.Cys591=
XM_011530489.1:c.1773C>T	XP_011528791.1:p.Cys591=
XM_011530489.2:c.1773C>T	XP_011528791.1:p.Cys591=
XM_011530490.1:c.1719C>T	XP_011528792.1:p.Cys573=
XM_011530490.3:c.1719C>T	XP_011528792.1:p.Cys573=
XM_011530491.1:c.1773C>T	XP_011528793.1:p.Cys591=
XM_011530491.3:c.1773C>T	XP_011528793.1:p.Cys591=
XM_011530492.1:c.1773C>T	XP_011528794.1:p.Cys591=
XM_011530492.2:c.1773C>T	XP_011528794.1:p.Cys591=
XM_011530493.1:c.1773C>T	XP_011528795.1:p.Cys591=
XM_011530493.3:c.1773C>T	XP_011528795.1:p.Cys591=
XM_011530494.1:c.981C>T	XP_011528796.1:p.Cys327=
XM_011530494.2:c.981C>T	XP_011528796.1:p.Cys327=
XM_011530495.1:c.1128C>T	XP_011528797.1:p.Cys376=
XM_011530495.2:c.1128C>T	XP_011528797.1:p.Cys376=
XM_011530496.1:c.981C>T	XP_011528798.1:p.Cys327=
XM_011530496.2:c.981C>T	XP_011528798.1:p.Cys327=
XM_017029045.2:c.1719C>T	XP_016884534.1:p.Cys573=
XM_017029046.2:c.1641C>T	XP_016884535.1:p.Cys547=
XM_017029047.2:c.1719C>T	XP_016884536.1:p.Cys573=
XM_017029052.2:c.1233C>T	XP_016884541.1:p.Cys411=
XM_017029053.1:c.1218C>T	XP_016884542.1:p.Cys406=
XM_017029056.2:c.846C>T	XP_016884545.1:p.Cys282=
XM_017029061.2:c.846C>T	XP_016884550.1:p.Cys282=
XM_017029062.2:c.846C>T	XP_016884551.1:p.Cys282=
XM_017029063.2:c.846C>T	XP_016884552.1:p.Cys282=
XM_017029064.2:c.846C>T	XP_016884553.1:p.Cys282=
XM_024452298.1:c.1014C>T	XP_024308066.1:p.Cys338=
XM_024452299.1:c.846C>T	XP_024308067.1:p.Cys282=
XM_024452300.1:c.846C>T	XP_024308068.1:p.Cys282=
XR_001755361.2:n.2349C>T
XR_001755364.1:n.2205C>T
XR_001755366.2:n.2878C>T
XR_002958721.1:n.2427C>T
XR_937947.1:n.2432C>T
XR_937947.2:n.2427C>T