Canonical Allele Identifier: CA513920329

Gene: HPS4

Linked Data

• MyVariant Identifiers: chr22:g.26853881G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26457915G>C , CM000684.2:g.26457915G>C	GRCh38
NC_000022.10:g.26853881G>C , CM000684.1:g.26853881G>C	GRCh37
NC_000022.9:g.25183881G>C	NCBI36
NG_009763.2:g.30949C>G , LRG_590:g.30949C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422379.3:c.1953C>G	ENSP00000415081.3:p.Val651=
ENST00000473782.2:c.1899C>G	ENSP00000514223.1:p.Val633=
ENST00000483631.2:c.1104C>G	ENSP00000514228.1:p.Val368=
ENST00000491142.2:c.1899C>G	ENSP00000514221.1:p.Val633=
ENST00000699226.1:n.4825C>G
ENST00000699227.1:c.*1243C>G	ENSP00000514220.1:n.*1243C>G
ENST00000699228.1:n.2449C>G
ENST00000699229.1:n.1316C>G
ENST00000699230.1:n.2622C>G
ENST00000699231.1:n.4911C>G
ENST00000699232.1:n.3255C>G
ENST00000699233.1:n.1770C>G
ENST00000699234.1:c.*1243C>G	ENSP00000514222.1:n.*1243C>G
ENST00000699235.1:c.1104C>G	ENSP00000514224.1:p.Val368=
ENST00000699236.1:c.*1088C>G	ENSP00000514225.1:n.*1088C>G
ENST00000699237.1:c.*1088C>G	ENSP00000514226.1:n.*1088C>G
ENST00000699238.1:c.*1442C>G	ENSP00000514227.1:n.*1442C>G
ENST00000699239.1:n.4653C>G
ENST00000699240.1:c.*1556C>G	ENSP00000514229.1:n.*1556C>G
ENST00000699241.1:c.*2091C>G	ENSP00000514230.1:n.*2091C>G
ENST00000699242.1:c.1809C>G	ENSP00000514231.1:p.Val603=
ENST00000699243.1:c.*1243C>G	ENSP00000514232.1:n.*1243C>G
ENST00000699244.1:c.1752C>G	ENSP00000514233.1:p.Val584=
ENST00000699245.1:n.1191C>G
ENST00000699246.1:c.*1270C>G	ENSP00000514234.1:n.*1270C>G
ENST00000699247.1:c.855C>G	ENSP00000514235.1:p.Val285=
ENST00000699248.1:n.3784-4511C>G
ENST00000699249.1:c.*1058-4511C>G	ENSP00000514236.1:n.*1058-4511C>G
ENST00000699250.1:c.1714-4511C>G	ENSP00000514237.1:n.1714-4511C>G
ENST00000699251.1:c.1899C>G	ENSP00000514238.1:p.Val633=
ENST00000699252.1:n.2449C>G
ENST00000398145.7:c.1899C>G MANE Select	ENSP00000381213.2:p.Val633=
ENST00000336873.9:c.1899C>G	ENSP00000338457.5:p.Val633=
ENST00000398145.6:c.1899C>G	ENSP00000381213.2:p.Val633=
ENST00000402105.7:c.1884C>G	ENSP00000384185.3:p.Val628=
ENST00000429411.5:c.*1471C>G	ENSP00000399705.1:n.*1471C>G
ENST00000439453.5:c.*1417C>G	ENSP00000406764.1:n.*1417C>G
ENST00000464362.5:c.*2230C>G	ENSP00000430291.1:n.*2230C>G
ENST00000466781.5:n.4758C>G
ENST00000485842.5:n.590C>G
ENST00000493455.6:n.462C>G
ENST00000496385.5:n.2480-4511C>G
ENST00000519774.5:n.285C>G
NM_022081.5:c.1899C>G , LRG_590t1:c.1899C>G	NP_071364.4:p.Val633=
NM_152841.2:c.1884C>G , LRG_590t2:c.1884C>G	NP_690054.1:p.Val628=
NR_073135.1:n.2585C>G
NR_073136.1:n.2347C>G
XM_006724353.2:c.1953C>G	XP_006724416.1:p.Val651=
XM_006724354.2:c.1953C>G	XP_006724417.1:p.Val651=
XM_006724360.2:c.1386C>G	XP_006724423.1:p.Val462=
XM_011530485.1:c.2031C>G	XP_011528787.1:p.Val677=
XM_011530486.1:c.2031C>G	XP_011528788.1:p.Val677=
XM_011530487.1:c.2031C>G	XP_011528789.1:p.Val677=
XM_011530488.1:c.2031C>G	XP_011528790.1:p.Val677=
XM_011530489.1:c.2031C>G	XP_011528791.1:p.Val677=
XM_011530490.1:c.1977C>G	XP_011528792.1:p.Val659=
XM_011530491.1:c.2031C>G	XP_011528793.1:p.Val677=
XM_011530492.1:c.2031C>G	XP_011528794.1:p.Val677=
XM_011530493.1:c.1846-4511C>G	XP_011528795.1:n.1846-4511C>G
XM_011530494.1:c.1239C>G	XP_011528796.1:p.Val413=
XM_011530495.1:c.1386C>G	XP_011528797.1:p.Val462=
XM_011530496.1:c.1239C>G	XP_011528798.1:p.Val413=
XR_937947.1:n.2690C>G
NM_001349896.1:c.1899C>G	NP_001336825.1:p.Val633=
NM_001349898.1:c.1899C>G	NP_001336827.1:p.Val633=
NM_001349899.1:c.1899C>G	NP_001336828.1:p.Val633=
NM_001349900.1:c.1953C>G	NP_001336829.1:p.Val651=
NM_001349901.1:c.1953C>G	NP_001336830.1:p.Val651=
NM_001349902.1:c.1714-4511C>G	NP_001336831.1:n.1714-4511C>G
NM_001349903.1:c.1714-4511C>G	NP_001336832.1:n.1714-4511C>G
NM_001349904.1:c.1899C>G	NP_001336833.1:p.Val633=
NM_001349905.1:c.1899C>G	NP_001336834.1:p.Val633=
NR_146311.1:n.2676C>G
NR_146312.1:n.2501C>G
NR_146313.1:n.2521C>G
NR_146314.1:n.2652C>G
NR_146315.1:n.2592C>G
NR_146316.1:n.2567C>G
XM_006724360.3:c.1386C>G	XP_006724423.1:p.Val462=
XM_011530485.2:c.2031C>G	XP_011528787.1:p.Val677=
XM_011530486.2:c.2031C>G	XP_011528788.1:p.Val677=
XM_011530487.2:c.2031C>G	XP_011528789.1:p.Val677=
XM_011530488.2:c.2031C>G	XP_011528790.1:p.Val677=
XM_011530489.2:c.2031C>G	XP_011528791.1:p.Val677=
XM_011530490.3:c.1977C>G	XP_011528792.1:p.Val659=
XM_011530491.3:c.2031C>G	XP_011528793.1:p.Val677=
XM_011530492.2:c.2031C>G	XP_011528794.1:p.Val677=
XM_011530493.3:c.1846-4511C>G	XP_011528795.1:n.1846-4511C>G
XM_011530494.2:c.1239C>G	XP_011528796.1:p.Val413=
XM_011530495.2:c.1386C>G	XP_011528797.1:p.Val462=
XM_011530496.2:c.1239C>G	XP_011528798.1:p.Val413=
XM_017029045.2:c.1977C>G	XP_016884534.1:p.Val659=
XM_017029046.2:c.1899C>G	XP_016884535.1:p.Val633=
XM_017029047.2:c.1792-4511C>G	XP_016884536.1:n.1792-4511C>G
XM_017029052.2:c.1491C>G	XP_016884541.1:p.Val497=
XM_017029053.1:c.1476C>G	XP_016884542.1:p.Val492=
XM_017029056.2:c.1104C>G	XP_016884545.1:p.Val368=
XM_017029061.2:c.1104C>G	XP_016884550.1:p.Val368=
XM_017029062.2:c.1104C>G	XP_016884551.1:p.Val368=
XM_017029063.2:c.1104C>G	XP_016884552.1:p.Val368=
XM_017029064.2:c.1104C>G	XP_016884553.1:p.Val368=
XM_024452298.1:c.1272C>G	XP_024308066.1:p.Val424=
XM_024452299.1:c.1104C>G	XP_024308067.1:p.Val368=
XM_024452300.1:c.1104C>G	XP_024308068.1:p.Val368=
XR_001755361.2:n.2607C>G
XR_001755364.1:n.2278-4511C>G
XR_001755366.2:n.3136C>G
XR_002958721.1:n.2500-4511C>G
XR_937947.2:n.2685C>G
NM_001349898.2:c.1899C>G	NP_001336827.1:p.Val633=
NM_001349899.2:c.1899C>G	NP_001336828.1:p.Val633=
NM_001349900.2:c.1953C>G	NP_001336829.1:p.Val651=
NM_001349903.2:c.1714-4511C>G	NP_001336832.1:n.1714-4511C>G
NM_001349904.2:c.1899C>G	NP_001336833.1:p.Val633=
NR_073136.2:n.2154C>G
NR_146311.2:n.2596C>G
NR_146313.2:n.2441C>G
NR_146315.2:n.2512C>G
NM_022081.6:c.1899C>G MANE Select	NP_071364.4:p.Val633=
NR_146316.2:n.2487C>G