Canonical Allele Identifier: CA411027344

Gene: HPS4

Linked Data

• MyVariant Identifiers: chr22:g.26860287G>C (hg19) ; chr22:g.26464321G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.26464321G>C , CM000684.2:g.26464321G>C	GRCh38
NC_000022.10:g.26860287G>C , CM000684.1:g.26860287G>C	GRCh37
NC_000022.9:g.25190287G>C	NCBI36
NG_009763.2:g.24543C>G , LRG_590:g.24543C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422379.3:c.1363C>G	ENSP00000415081.3:p.His455Asp
ENST00000473782.2:c.1309C>G	ENSP00000514223.1:p.His437Asp
ENST00000483631.2:c.514C>G	ENSP00000514228.1:p.His172Asp
ENST00000491142.2:c.1309C>G	ENSP00000514221.1:p.His437Asp
ENST00000699226.1:n.4235C>G
ENST00000699227.1:c.*653C>G	ENSP00000514220.1:n.*653C>G
ENST00000699228.1:n.1859C>G
ENST00000699229.1:n.726C>G
ENST00000699230.1:n.2032C>G
ENST00000699231.1:n.4321C>G
ENST00000699232.1:n.2665C>G
ENST00000699233.1:n.1180C>G
ENST00000699234.1:c.*653C>G	ENSP00000514222.1:n.*653C>G
ENST00000699235.1:c.514C>G	ENSP00000514224.1:p.His172Asp
ENST00000699236.1:c.*498C>G	ENSP00000514225.1:n.*498C>G
ENST00000699237.1:c.*498C>G	ENSP00000514226.1:n.*498C>G
ENST00000699238.1:c.*852C>G	ENSP00000514227.1:n.*852C>G
ENST00000699239.1:n.4063C>G
ENST00000699240.1:c.*966C>G	ENSP00000514229.1:n.*966C>G
ENST00000699241.1:c.*1501C>G	ENSP00000514230.1:n.*1501C>G
ENST00000699242.1:c.1219C>G	ENSP00000514231.1:p.His407Asp
ENST00000699243.1:c.*653C>G	ENSP00000514232.1:n.*653C>G
ENST00000699244.1:c.1162C>G	ENSP00000514233.1:p.His388Asp
ENST00000699246.1:c.*680C>G	ENSP00000514234.1:n.*680C>G
ENST00000699247.1:c.669+4230C>G	ENSP00000514235.1:n.669+4230C>G
ENST00000699248.1:n.3379C>G
ENST00000699249.1:c.*653C>G	ENSP00000514236.1:n.*653C>G
ENST00000699250.1:c.1309C>G	ENSP00000514237.1:p.His437Asp
ENST00000699251.1:c.1309C>G	ENSP00000514238.1:p.His437Asp
ENST00000699252.1:n.1859C>G
ENST00000398145.7:c.1309C>G MANE Select	ENSP00000381213.2:p.His437Asp
ENST00000336873.9:c.1309C>G	ENSP00000338457.5:p.His437Asp
ENST00000398145.6:c.1309C>G	ENSP00000381213.2:p.His437Asp
ENST00000402105.7:c.1294C>G	ENSP00000384185.3:p.His432Asp
ENST00000422379.2:c.1363C>G	ENSP00000415081.2:p.His455Asp
ENST00000429411.5:c.*881C>G	ENSP00000399705.1:n.*881C>G
ENST00000439453.5:c.*827C>G	ENSP00000406764.1:n.*827C>G
ENST00000464362.5:c.*1640C>G	ENSP00000430291.1:n.*1640C>G
ENST00000466781.5:n.4168C>G
ENST00000485842.5:n.404+4230C>G
ENST00000496385.5:n.2075C>G
NM_022081.5:c.1309C>G , LRG_590t1:c.1309C>G	NP_071364.4:p.His437Asp
NM_152841.2:c.1294C>G , LRG_590t2:c.1294C>G	NP_690054.1:p.His432Asp
NR_073135.1:n.1995C>G
NR_073136.1:n.1757C>G
XM_006724353.2:c.1363C>G	XP_006724416.1:p.His455Asp
XM_006724354.2:c.1363C>G	XP_006724417.1:p.His455Asp
XM_006724360.2:c.796C>G	XP_006724423.1:p.His266Asp
XM_011530485.1:c.1441C>G	XP_011528787.1:p.His481Asp
XM_011530486.1:c.1441C>G	XP_011528788.1:p.His481Asp
XM_011530487.1:c.1441C>G	XP_011528789.1:p.His481Asp
XM_011530488.1:c.1441C>G	XP_011528790.1:p.His481Asp
XM_011530489.1:c.1441C>G	XP_011528791.1:p.His481Asp
XM_011530490.1:c.1387C>G	XP_011528792.1:p.His463Asp
XM_011530491.1:c.1441C>G	XP_011528793.1:p.His481Asp
XM_011530492.1:c.1441C>G	XP_011528794.1:p.His481Asp
XM_011530493.1:c.1441C>G	XP_011528795.1:p.His481Asp
XM_011530494.1:c.649C>G	XP_011528796.1:p.His217Asp
XM_011530495.1:c.796C>G	XP_011528797.1:p.His266Asp
XM_011530496.1:c.649C>G	XP_011528798.1:p.His217Asp
XR_937947.1:n.2100C>G
NM_001349896.1:c.1309C>G	NP_001336825.1:p.His437Asp
NM_001349898.1:c.1309C>G	NP_001336827.1:p.His437Asp
NM_001349899.1:c.1309C>G	NP_001336828.1:p.His437Asp
NM_001349900.1:c.1363C>G	NP_001336829.1:p.His455Asp
NM_001349901.1:c.1363C>G	NP_001336830.1:p.His455Asp
NM_001349902.1:c.1309C>G	NP_001336831.1:p.His437Asp
NM_001349903.1:c.1309C>G	NP_001336832.1:p.His437Asp
NM_001349904.1:c.1309C>G	NP_001336833.1:p.His437Asp
NM_001349905.1:c.1309C>G	NP_001336834.1:p.His437Asp
NR_146311.1:n.2086C>G
NR_146312.1:n.1911C>G
NR_146313.1:n.1931C>G
NR_146314.1:n.2062C>G
NR_146315.1:n.2002C>G
NR_146316.1:n.1977C>G
XM_006724360.3:c.796C>G	XP_006724423.1:p.His266Asp
XM_011530485.2:c.1441C>G	XP_011528787.1:p.His481Asp
XM_011530486.2:c.1441C>G	XP_011528788.1:p.His481Asp
XM_011530487.2:c.1441C>G	XP_011528789.1:p.His481Asp
XM_011530488.2:c.1441C>G	XP_011528790.1:p.His481Asp
XM_011530489.2:c.1441C>G	XP_011528791.1:p.His481Asp
XM_011530490.3:c.1387C>G	XP_011528792.1:p.His463Asp
XM_011530491.3:c.1441C>G	XP_011528793.1:p.His481Asp
XM_011530492.2:c.1441C>G	XP_011528794.1:p.His481Asp
XM_011530493.3:c.1441C>G	XP_011528795.1:p.His481Asp
XM_011530494.2:c.649C>G	XP_011528796.1:p.His217Asp
XM_011530495.2:c.796C>G	XP_011528797.1:p.His266Asp
XM_011530496.2:c.649C>G	XP_011528798.1:p.His217Asp
XM_017029045.2:c.1387C>G	XP_016884534.1:p.His463Asp
XM_017029046.2:c.1309C>G	XP_016884535.1:p.His437Asp
XM_017029047.2:c.1387C>G	XP_016884536.1:p.His463Asp
XM_017029052.2:c.901C>G	XP_016884541.1:p.His301Asp
XM_017029053.1:c.886C>G	XP_016884542.1:p.His296Asp
XM_017029056.2:c.514C>G	XP_016884545.1:p.His172Asp
XM_017029061.2:c.514C>G	XP_016884550.1:p.His172Asp
XM_017029062.2:c.514C>G	XP_016884551.1:p.His172Asp
XM_017029063.2:c.514C>G	XP_016884552.1:p.His172Asp
XM_017029064.2:c.514C>G	XP_016884553.1:p.His172Asp
XM_024452298.1:c.682C>G	XP_024308066.1:p.His228Asp
XM_024452299.1:c.514C>G	XP_024308067.1:p.His172Asp
XM_024452300.1:c.514C>G	XP_024308068.1:p.His172Asp
XR_001755361.2:n.2017C>G
XR_001755364.1:n.1873C>G
XR_001755366.2:n.2546C>G
XR_002958721.1:n.2095C>G
XR_937947.2:n.2095C>G
NM_001349898.2:c.1309C>G	NP_001336827.1:p.His437Asp
NM_001349899.2:c.1309C>G	NP_001336828.1:p.His437Asp
NM_001349900.2:c.1363C>G	NP_001336829.1:p.His455Asp
NM_001349903.2:c.1309C>G	NP_001336832.1:p.His437Asp
NM_001349904.2:c.1309C>G	NP_001336833.1:p.His437Asp
NR_073136.2:n.1564C>G
NR_146311.2:n.2006C>G
NR_146313.2:n.1851C>G
NR_146315.2:n.1922C>G
NM_022081.6:c.1309C>G MANE Select	NP_071364.4:p.His437Asp
NR_146316.2:n.1897C>G