Canonical Allele Identifier: CA514164260

Gene: HPS4

Linked Data

• MyVariant Identifiers: chr22:g.26860188A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26464222A>G , CM000684.2:g.26464222A>G	GRCh38
NC_000022.10:g.26860188A>G , CM000684.1:g.26860188A>G	GRCh37
NC_000022.9:g.25190188A>G	NCBI36
NG_009763.2:g.24642T>C , LRG_590:g.24642T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422379.3:c.1462T>C	ENSP00000415081.3:p.Leu488=
ENST00000473782.2:c.1408T>C	ENSP00000514223.1:p.Leu470=
ENST00000483631.2:c.613T>C	ENSP00000514228.1:p.Leu205=
ENST00000491142.2:c.1408T>C	ENSP00000514221.1:p.Leu470=
ENST00000699226.1:n.4334T>C
ENST00000699227.1:c.*752T>C	ENSP00000514220.1:n.*752T>C
ENST00000699228.1:n.1958T>C
ENST00000699229.1:n.825T>C
ENST00000699230.1:n.2131T>C
ENST00000699231.1:n.4420T>C
ENST00000699232.1:n.2764T>C
ENST00000699233.1:n.1279T>C
ENST00000699234.1:c.*752T>C	ENSP00000514222.1:n.*752T>C
ENST00000699235.1:c.613T>C	ENSP00000514224.1:p.Leu205=
ENST00000699236.1:c.*597T>C	ENSP00000514225.1:n.*597T>C
ENST00000699237.1:c.*597T>C	ENSP00000514226.1:n.*597T>C
ENST00000699238.1:c.*951T>C	ENSP00000514227.1:n.*951T>C
ENST00000699239.1:n.4162T>C
ENST00000699240.1:c.*1065T>C	ENSP00000514229.1:n.*1065T>C
ENST00000699241.1:c.*1600T>C	ENSP00000514230.1:n.*1600T>C
ENST00000699242.1:c.1318T>C	ENSP00000514231.1:p.Leu440=
ENST00000699243.1:c.*752T>C	ENSP00000514232.1:n.*752T>C
ENST00000699244.1:c.1261T>C	ENSP00000514233.1:p.Leu421=
ENST00000699246.1:c.*779T>C	ENSP00000514234.1:n.*779T>C
ENST00000699247.1:c.669+4329T>C	ENSP00000514235.1:n.669+4329T>C
ENST00000699248.1:n.3478T>C
ENST00000699249.1:c.*752T>C	ENSP00000514236.1:n.*752T>C
ENST00000699250.1:c.1408T>C	ENSP00000514237.1:p.Leu470=
ENST00000699251.1:c.1408T>C	ENSP00000514238.1:p.Leu470=
ENST00000699252.1:n.1958T>C
ENST00000398145.7:c.1408T>C MANE Select	ENSP00000381213.2:p.Leu470=
ENST00000336873.9:c.1408T>C	ENSP00000338457.5:p.Leu470=
ENST00000398145.6:c.1408T>C	ENSP00000381213.2:p.Leu470=
ENST00000402105.7:c.1393T>C	ENSP00000384185.3:p.Leu465=
ENST00000429411.5:c.*980T>C	ENSP00000399705.1:n.*980T>C
ENST00000439453.5:c.*926T>C	ENSP00000406764.1:n.*926T>C
ENST00000464362.5:c.*1739T>C	ENSP00000430291.1:n.*1739T>C
ENST00000466781.5:n.4267T>C
ENST00000485842.5:n.404+4329T>C
ENST00000496385.5:n.2174T>C
NM_022081.5:c.1408T>C , LRG_590t1:c.1408T>C	NP_071364.4:p.Leu470=
NM_152841.2:c.1393T>C , LRG_590t2:c.1393T>C	NP_690054.1:p.Leu465=
NR_073135.1:n.2094T>C
NR_073136.1:n.1856T>C
XM_006724353.2:c.1462T>C	XP_006724416.1:p.Leu488=
XM_006724354.2:c.1462T>C	XP_006724417.1:p.Leu488=
XM_006724360.2:c.895T>C	XP_006724423.1:p.Leu299=
XM_011530485.1:c.1540T>C	XP_011528787.1:p.Leu514=
XM_011530486.1:c.1540T>C	XP_011528788.1:p.Leu514=
XM_011530487.1:c.1540T>C	XP_011528789.1:p.Leu514=
XM_011530488.1:c.1540T>C	XP_011528790.1:p.Leu514=
XM_011530489.1:c.1540T>C	XP_011528791.1:p.Leu514=
XM_011530490.1:c.1486T>C	XP_011528792.1:p.Leu496=
XM_011530491.1:c.1540T>C	XP_011528793.1:p.Leu514=
XM_011530492.1:c.1540T>C	XP_011528794.1:p.Leu514=
XM_011530493.1:c.1540T>C	XP_011528795.1:p.Leu514=
XM_011530494.1:c.748T>C	XP_011528796.1:p.Leu250=
XM_011530495.1:c.895T>C	XP_011528797.1:p.Leu299=
XM_011530496.1:c.748T>C	XP_011528798.1:p.Leu250=
XR_937947.1:n.2199T>C
NM_001349896.1:c.1408T>C	NP_001336825.1:p.Leu470=
NM_001349898.1:c.1408T>C	NP_001336827.1:p.Leu470=
NM_001349899.1:c.1408T>C	NP_001336828.1:p.Leu470=
NM_001349900.1:c.1462T>C	NP_001336829.1:p.Leu488=
NM_001349901.1:c.1462T>C	NP_001336830.1:p.Leu488=
NM_001349902.1:c.1408T>C	NP_001336831.1:p.Leu470=
NM_001349903.1:c.1408T>C	NP_001336832.1:p.Leu470=
NM_001349904.1:c.1408T>C	NP_001336833.1:p.Leu470=
NM_001349905.1:c.1408T>C	NP_001336834.1:p.Leu470=
NR_146311.1:n.2185T>C
NR_146312.1:n.2010T>C
NR_146313.1:n.2030T>C
NR_146314.1:n.2161T>C
NR_146315.1:n.2101T>C
NR_146316.1:n.2076T>C
XM_006724360.3:c.895T>C	XP_006724423.1:p.Leu299=
XM_011530485.2:c.1540T>C	XP_011528787.1:p.Leu514=
XM_011530486.2:c.1540T>C	XP_011528788.1:p.Leu514=
XM_011530487.2:c.1540T>C	XP_011528789.1:p.Leu514=
XM_011530488.2:c.1540T>C	XP_011528790.1:p.Leu514=
XM_011530489.2:c.1540T>C	XP_011528791.1:p.Leu514=
XM_011530490.3:c.1486T>C	XP_011528792.1:p.Leu496=
XM_011530491.3:c.1540T>C	XP_011528793.1:p.Leu514=
XM_011530492.2:c.1540T>C	XP_011528794.1:p.Leu514=
XM_011530493.3:c.1540T>C	XP_011528795.1:p.Leu514=
XM_011530494.2:c.748T>C	XP_011528796.1:p.Leu250=
XM_011530495.2:c.895T>C	XP_011528797.1:p.Leu299=
XM_011530496.2:c.748T>C	XP_011528798.1:p.Leu250=
XM_017029045.2:c.1486T>C	XP_016884534.1:p.Leu496=
XM_017029046.2:c.1408T>C	XP_016884535.1:p.Leu470=
XM_017029047.2:c.1486T>C	XP_016884536.1:p.Leu496=
XM_017029052.2:c.1000T>C	XP_016884541.1:p.Leu334=
XM_017029053.1:c.985T>C	XP_016884542.1:p.Leu329=
XM_017029056.2:c.613T>C	XP_016884545.1:p.Leu205=
XM_017029061.2:c.613T>C	XP_016884550.1:p.Leu205=
XM_017029062.2:c.613T>C	XP_016884551.1:p.Leu205=
XM_017029063.2:c.613T>C	XP_016884552.1:p.Leu205=
XM_017029064.2:c.613T>C	XP_016884553.1:p.Leu205=
XM_024452298.1:c.781T>C	XP_024308066.1:p.Leu261=
XM_024452299.1:c.613T>C	XP_024308067.1:p.Leu205=
XM_024452300.1:c.613T>C	XP_024308068.1:p.Leu205=
XR_001755361.2:n.2116T>C
XR_001755364.1:n.1972T>C
XR_001755366.2:n.2645T>C
XR_002958721.1:n.2194T>C
XR_937947.2:n.2194T>C
NM_001349898.2:c.1408T>C	NP_001336827.1:p.Leu470=
NM_001349899.2:c.1408T>C	NP_001336828.1:p.Leu470=
NM_001349900.2:c.1462T>C	NP_001336829.1:p.Leu488=
NM_001349903.2:c.1408T>C	NP_001336832.1:p.Leu470=
NM_001349904.2:c.1408T>C	NP_001336833.1:p.Leu470=
NR_073136.2:n.1663T>C
NR_146311.2:n.2105T>C
NR_146313.2:n.1950T>C
NR_146315.2:n.2021T>C
NM_022081.6:c.1408T>C MANE Select	NP_071364.4:p.Leu470=
NR_146316.2:n.1996T>C