Canonical Allele Identifier: CA10163321

Gene: HPS4

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26464175C>T , CM000684.2:g.26464175C>T	GRCh38
NC_000022.10:g.26860141C>T , CM000684.1:g.26860141C>T	GRCh37
NC_000022.9:g.25190141C>T	NCBI36
NG_009763.2:g.24689G>A , LRG_590:g.24689G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022081.6:c.1455G>A MANE Select	NP_071364.4:p.Thr485=
ENST00000398145.7:c.1455G>A MANE Select	ENSP00000381213.2:p.Thr485=
NM_001349896.1:c.1455G>A	NP_001336825.1:p.Thr485=
NM_001349898.1:c.1455G>A	NP_001336827.1:p.Thr485=
NM_001349898.2:c.1455G>A	NP_001336827.1:p.Thr485=
NM_001349899.1:c.1455G>A	NP_001336828.1:p.Thr485=
NM_001349899.2:c.1455G>A	NP_001336828.1:p.Thr485=
NM_001349900.1:c.1509G>A	NP_001336829.1:p.Thr503=
NM_001349900.2:c.1509G>A	NP_001336829.1:p.Thr503=
NM_001349901.1:c.1509G>A	NP_001336830.1:p.Thr503=
NM_001349902.1:c.1455G>A	NP_001336831.1:p.Thr485=
NM_001349903.1:c.1455G>A	NP_001336832.1:p.Thr485=
NM_001349903.2:c.1455G>A	NP_001336832.1:p.Thr485=
NM_001349904.1:c.1455G>A	NP_001336833.1:p.Thr485=
NM_001349904.2:c.1455G>A	NP_001336833.1:p.Thr485=
NM_001349905.1:c.1455G>A	NP_001336834.1:p.Thr485=
NM_022081.5:c.1455G>A , LRG_590t1:c.1455G>A	NP_071364.4:p.Thr485=
NM_152841.2:c.1440G>A , LRG_590t2:c.1440G>A	NP_690054.1:p.Thr480=
NR_073135.1:n.2141G>A
NR_073136.1:n.1903G>A
NR_073136.2:n.1710G>A
NR_146311.1:n.2232G>A
NR_146311.2:n.2152G>A
NR_146312.1:n.2057G>A
NR_146313.1:n.2077G>A
NR_146313.2:n.1997G>A
NR_146314.1:n.2208G>A
NR_146315.1:n.2148G>A
NR_146315.2:n.2068G>A
NR_146316.1:n.2123G>A
NR_146316.2:n.2043G>A
ENST00000336873.9:c.1455G>A	ENSP00000338457.5:p.Thr485=
ENST00000398145.6:c.1455G>A	ENSP00000381213.2:p.Thr485=
ENST00000402105.7:c.1440G>A	ENSP00000384185.3:p.Thr480=
ENST00000422379.3:c.1509G>A	ENSP00000415081.3:p.Thr503=
ENST00000429411.5:c.*1027G>A	ENSP00000399705.1:n.*1027G>A
ENST00000439453.5:c.*973G>A	ENSP00000406764.1:n.*973G>A
ENST00000464362.5:c.*1786G>A	ENSP00000430291.1:n.*1786G>A
ENST00000466781.5:n.4314G>A
ENST00000473782.2:c.1455G>A	ENSP00000514223.1:p.Thr485=
ENST00000483631.2:c.660G>A	ENSP00000514228.1:p.Thr220=
ENST00000485842.5:n.404+4376G>A
ENST00000491142.2:c.1455G>A	ENSP00000514221.1:p.Thr485=
ENST00000493455.6:n.18G>A
ENST00000496385.5:n.2221G>A
ENST00000699226.1:n.4381G>A
ENST00000699227.1:c.*799G>A	ENSP00000514220.1:n.*799G>A
ENST00000699228.1:n.2005G>A
ENST00000699229.1:n.872G>A
ENST00000699230.1:n.2178G>A
ENST00000699231.1:n.4467G>A
ENST00000699232.1:n.2811G>A
ENST00000699233.1:n.1326G>A
ENST00000699234.1:c.*799G>A	ENSP00000514222.1:n.*799G>A
ENST00000699235.1:c.660G>A	ENSP00000514224.1:p.Thr220=
ENST00000699236.1:c.*644G>A	ENSP00000514225.1:n.*644G>A
ENST00000699237.1:c.*644G>A	ENSP00000514226.1:n.*644G>A
ENST00000699238.1:c.*998G>A	ENSP00000514227.1:n.*998G>A
ENST00000699239.1:n.4209G>A
ENST00000699240.1:c.*1112G>A	ENSP00000514229.1:n.*1112G>A
ENST00000699241.1:c.*1647G>A	ENSP00000514230.1:n.*1647G>A
ENST00000699242.1:c.1365G>A	ENSP00000514231.1:p.Thr455=
ENST00000699243.1:c.*799G>A	ENSP00000514232.1:n.*799G>A
ENST00000699244.1:c.1308G>A	ENSP00000514233.1:p.Thr436=
ENST00000699246.1:c.*826G>A	ENSP00000514234.1:n.*826G>A
ENST00000699247.1:c.669+4376G>A	ENSP00000514235.1:n.669+4376G>A
ENST00000699248.1:n.3525G>A
ENST00000699249.1:c.*799G>A	ENSP00000514236.1:n.*799G>A
ENST00000699250.1:c.1455G>A	ENSP00000514237.1:p.Thr485=
ENST00000699251.1:c.1455G>A	ENSP00000514238.1:p.Thr485=
ENST00000699252.1:n.2005G>A
XM_006724353.2:c.1509G>A	XP_006724416.1:p.Thr503=
XM_006724354.2:c.1509G>A	XP_006724417.1:p.Thr503=
XM_006724360.2:c.942G>A	XP_006724423.1:p.Thr314=
XM_006724360.3:c.942G>A	XP_006724423.1:p.Thr314=
XM_011530485.1:c.1587G>A	XP_011528787.1:p.Thr529=
XM_011530485.2:c.1587G>A	XP_011528787.1:p.Thr529=
XM_011530486.1:c.1587G>A	XP_011528788.1:p.Thr529=
XM_011530486.2:c.1587G>A	XP_011528788.1:p.Thr529=
XM_011530487.1:c.1587G>A	XP_011528789.1:p.Thr529=
XM_011530487.2:c.1587G>A	XP_011528789.1:p.Thr529=
XM_011530488.1:c.1587G>A	XP_011528790.1:p.Thr529=
XM_011530488.2:c.1587G>A	XP_011528790.1:p.Thr529=
XM_011530489.1:c.1587G>A	XP_011528791.1:p.Thr529=
XM_011530489.2:c.1587G>A	XP_011528791.1:p.Thr529=
XM_011530490.1:c.1533G>A	XP_011528792.1:p.Thr511=
XM_011530490.3:c.1533G>A	XP_011528792.1:p.Thr511=
XM_011530491.1:c.1587G>A	XP_011528793.1:p.Thr529=
XM_011530491.3:c.1587G>A	XP_011528793.1:p.Thr529=
XM_011530492.1:c.1587G>A	XP_011528794.1:p.Thr529=
XM_011530492.2:c.1587G>A	XP_011528794.1:p.Thr529=
XM_011530493.1:c.1587G>A	XP_011528795.1:p.Thr529=
XM_011530493.3:c.1587G>A	XP_011528795.1:p.Thr529=
XM_011530494.1:c.795G>A	XP_011528796.1:p.Thr265=
XM_011530494.2:c.795G>A	XP_011528796.1:p.Thr265=
XM_011530495.1:c.942G>A	XP_011528797.1:p.Thr314=
XM_011530495.2:c.942G>A	XP_011528797.1:p.Thr314=
XM_011530496.1:c.795G>A	XP_011528798.1:p.Thr265=
XM_011530496.2:c.795G>A	XP_011528798.1:p.Thr265=
XM_017029045.2:c.1533G>A	XP_016884534.1:p.Thr511=
XM_017029046.2:c.1455G>A	XP_016884535.1:p.Thr485=
XM_017029047.2:c.1533G>A	XP_016884536.1:p.Thr511=
XM_017029052.2:c.1047G>A	XP_016884541.1:p.Thr349=
XM_017029053.1:c.1032G>A	XP_016884542.1:p.Thr344=
XM_017029056.2:c.660G>A	XP_016884545.1:p.Thr220=
XM_017029061.2:c.660G>A	XP_016884550.1:p.Thr220=
XM_017029062.2:c.660G>A	XP_016884551.1:p.Thr220=
XM_017029063.2:c.660G>A	XP_016884552.1:p.Thr220=
XM_017029064.2:c.660G>A	XP_016884553.1:p.Thr220=
XM_024452298.1:c.828G>A	XP_024308066.1:p.Thr276=
XM_024452299.1:c.660G>A	XP_024308067.1:p.Thr220=
XM_024452300.1:c.660G>A	XP_024308068.1:p.Thr220=
XR_001755361.2:n.2163G>A
XR_001755364.1:n.2019G>A
XR_001755366.2:n.2692G>A
XR_002958721.1:n.2241G>A
XR_937947.1:n.2246G>A
XR_937947.2:n.2241G>A