Canonical Allele Identifier: CA514164142

Gene: HPS4

Linked Data

• MyVariant Identifiers: chr22:g.26860123A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26464157A>G , CM000684.2:g.26464157A>G	GRCh38
NC_000022.10:g.26860123A>G , CM000684.1:g.26860123A>G	GRCh37
NC_000022.9:g.25190123A>G	NCBI36
NG_009763.2:g.24707T>C , LRG_590:g.24707T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422379.3:c.1527T>C	ENSP00000415081.3:p.Asp509=
ENST00000473782.2:c.1473T>C	ENSP00000514223.1:p.Asp491=
ENST00000483631.2:c.678T>C	ENSP00000514228.1:p.Asp226=
ENST00000491142.2:c.1473T>C	ENSP00000514221.1:p.Asp491=
ENST00000699226.1:n.4399T>C
ENST00000699227.1:c.*817T>C	ENSP00000514220.1:n.*817T>C
ENST00000699228.1:n.2023T>C
ENST00000699229.1:n.890T>C
ENST00000699230.1:n.2196T>C
ENST00000699231.1:n.4485T>C
ENST00000699232.1:n.2829T>C
ENST00000699233.1:n.1344T>C
ENST00000699234.1:c.*817T>C	ENSP00000514222.1:n.*817T>C
ENST00000699235.1:c.678T>C	ENSP00000514224.1:p.Asp226=
ENST00000699236.1:c.*662T>C	ENSP00000514225.1:n.*662T>C
ENST00000699237.1:c.*662T>C	ENSP00000514226.1:n.*662T>C
ENST00000699238.1:c.*1016T>C	ENSP00000514227.1:n.*1016T>C
ENST00000699239.1:n.4227T>C
ENST00000699240.1:c.*1130T>C	ENSP00000514229.1:n.*1130T>C
ENST00000699241.1:c.*1665T>C	ENSP00000514230.1:n.*1665T>C
ENST00000699242.1:c.1383T>C	ENSP00000514231.1:p.Asp461=
ENST00000699243.1:c.*817T>C	ENSP00000514232.1:n.*817T>C
ENST00000699244.1:c.1326T>C	ENSP00000514233.1:p.Asp442=
ENST00000699246.1:c.*844T>C	ENSP00000514234.1:n.*844T>C
ENST00000699247.1:c.669+4394T>C	ENSP00000514235.1:n.669+4394T>C
ENST00000699248.1:n.3543T>C
ENST00000699249.1:c.*817T>C	ENSP00000514236.1:n.*817T>C
ENST00000699250.1:c.1473T>C	ENSP00000514237.1:p.Asp491=
ENST00000699251.1:c.1473T>C	ENSP00000514238.1:p.Asp491=
ENST00000699252.1:n.2023T>C
ENST00000398145.7:c.1473T>C MANE Select	ENSP00000381213.2:p.Asp491=
ENST00000336873.9:c.1473T>C	ENSP00000338457.5:p.Asp491=
ENST00000398145.6:c.1473T>C	ENSP00000381213.2:p.Asp491=
ENST00000402105.7:c.1458T>C	ENSP00000384185.3:p.Asp486=
ENST00000429411.5:c.*1045T>C	ENSP00000399705.1:n.*1045T>C
ENST00000439453.5:c.*991T>C	ENSP00000406764.1:n.*991T>C
ENST00000464362.5:c.*1804T>C	ENSP00000430291.1:n.*1804T>C
ENST00000466781.5:n.4332T>C
ENST00000485842.5:n.404+4394T>C
ENST00000493455.6:n.36T>C
ENST00000496385.5:n.2239T>C
NM_022081.5:c.1473T>C , LRG_590t1:c.1473T>C	NP_071364.4:p.Asp491=
NM_152841.2:c.1458T>C , LRG_590t2:c.1458T>C	NP_690054.1:p.Asp486=
NR_073135.1:n.2159T>C
NR_073136.1:n.1921T>C
XM_006724353.2:c.1527T>C	XP_006724416.1:p.Asp509=
XM_006724354.2:c.1527T>C	XP_006724417.1:p.Asp509=
XM_006724360.2:c.960T>C	XP_006724423.1:p.Asp320=
XM_011530485.1:c.1605T>C	XP_011528787.1:p.Asp535=
XM_011530486.1:c.1605T>C	XP_011528788.1:p.Asp535=
XM_011530487.1:c.1605T>C	XP_011528789.1:p.Asp535=
XM_011530488.1:c.1605T>C	XP_011528790.1:p.Asp535=
XM_011530489.1:c.1605T>C	XP_011528791.1:p.Asp535=
XM_011530490.1:c.1551T>C	XP_011528792.1:p.Asp517=
XM_011530491.1:c.1605T>C	XP_011528793.1:p.Asp535=
XM_011530492.1:c.1605T>C	XP_011528794.1:p.Asp535=
XM_011530493.1:c.1605T>C	XP_011528795.1:p.Asp535=
XM_011530494.1:c.813T>C	XP_011528796.1:p.Asp271=
XM_011530495.1:c.960T>C	XP_011528797.1:p.Asp320=
XM_011530496.1:c.813T>C	XP_011528798.1:p.Asp271=
XR_937947.1:n.2264T>C
NM_001349896.1:c.1473T>C	NP_001336825.1:p.Asp491=
NM_001349898.1:c.1473T>C	NP_001336827.1:p.Asp491=
NM_001349899.1:c.1473T>C	NP_001336828.1:p.Asp491=
NM_001349900.1:c.1527T>C	NP_001336829.1:p.Asp509=
NM_001349901.1:c.1527T>C	NP_001336830.1:p.Asp509=
NM_001349902.1:c.1473T>C	NP_001336831.1:p.Asp491=
NM_001349903.1:c.1473T>C	NP_001336832.1:p.Asp491=
NM_001349904.1:c.1473T>C	NP_001336833.1:p.Asp491=
NM_001349905.1:c.1473T>C	NP_001336834.1:p.Asp491=
NR_146311.1:n.2250T>C
NR_146312.1:n.2075T>C
NR_146313.1:n.2095T>C
NR_146314.1:n.2226T>C
NR_146315.1:n.2166T>C
NR_146316.1:n.2141T>C
XM_006724360.3:c.960T>C	XP_006724423.1:p.Asp320=
XM_011530485.2:c.1605T>C	XP_011528787.1:p.Asp535=
XM_011530486.2:c.1605T>C	XP_011528788.1:p.Asp535=
XM_011530487.2:c.1605T>C	XP_011528789.1:p.Asp535=
XM_011530488.2:c.1605T>C	XP_011528790.1:p.Asp535=
XM_011530489.2:c.1605T>C	XP_011528791.1:p.Asp535=
XM_011530490.3:c.1551T>C	XP_011528792.1:p.Asp517=
XM_011530491.3:c.1605T>C	XP_011528793.1:p.Asp535=
XM_011530492.2:c.1605T>C	XP_011528794.1:p.Asp535=
XM_011530493.3:c.1605T>C	XP_011528795.1:p.Asp535=
XM_011530494.2:c.813T>C	XP_011528796.1:p.Asp271=
XM_011530495.2:c.960T>C	XP_011528797.1:p.Asp320=
XM_011530496.2:c.813T>C	XP_011528798.1:p.Asp271=
XM_017029045.2:c.1551T>C	XP_016884534.1:p.Asp517=
XM_017029046.2:c.1473T>C	XP_016884535.1:p.Asp491=
XM_017029047.2:c.1551T>C	XP_016884536.1:p.Asp517=
XM_017029052.2:c.1065T>C	XP_016884541.1:p.Asp355=
XM_017029053.1:c.1050T>C	XP_016884542.1:p.Asp350=
XM_017029056.2:c.678T>C	XP_016884545.1:p.Asp226=
XM_017029061.2:c.678T>C	XP_016884550.1:p.Asp226=
XM_017029062.2:c.678T>C	XP_016884551.1:p.Asp226=
XM_017029063.2:c.678T>C	XP_016884552.1:p.Asp226=
XM_017029064.2:c.678T>C	XP_016884553.1:p.Asp226=
XM_024452298.1:c.846T>C	XP_024308066.1:p.Asp282=
XM_024452299.1:c.678T>C	XP_024308067.1:p.Asp226=
XM_024452300.1:c.678T>C	XP_024308068.1:p.Asp226=
XR_001755361.2:n.2181T>C
XR_001755364.1:n.2037T>C
XR_001755366.2:n.2710T>C
XR_002958721.1:n.2259T>C
XR_937947.2:n.2259T>C
NM_001349898.2:c.1473T>C	NP_001336827.1:p.Asp491=
NM_001349899.2:c.1473T>C	NP_001336828.1:p.Asp491=
NM_001349900.2:c.1527T>C	NP_001336829.1:p.Asp509=
NM_001349903.2:c.1473T>C	NP_001336832.1:p.Asp491=
NM_001349904.2:c.1473T>C	NP_001336833.1:p.Asp491=
NR_073136.2:n.1728T>C
NR_146311.2:n.2170T>C
NR_146313.2:n.2015T>C
NR_146315.2:n.2086T>C
NM_022081.6:c.1473T>C MANE Select	NP_071364.4:p.Asp491=
NR_146316.2:n.2061T>C