Canonical Allele Identifier: CA5910141
Gene: HPS5 HGNC NCBI

Linked Data

ClinVar Variation Id: 431164
dbSNP Id: rs766602179

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18296887del , CM000673.2:g.18296887del GRCh38
NC_000011.9:g.18318434del , CM000673.1:g.18318434del GRCh37
NC_000011.8:g.18275010del NCBI36
NG_008877.1:g.30290del , LRG_586:g.30290del

Transcript Alleles

HGVS Amino-acid change
ENST00000349215.8:c.1423del MANE Select ENSP00000265967.5:p.Leu475SerfsTer?
ENST00000349215.7:c.1423del ENSP00000265967.5:p.Leu475SerfsTer?
ENST00000396253.7:c.1081del ENSP00000379552.3:p.Leu361SerfsTer?
ENST00000438420.6:c.1081del ENSP00000399590.2:p.Leu361SerfsTer?
ENST00000531848.1:c.1081del ENSP00000431758.1:p.Leu361SerfsTer?
NM_007216.3:c.1081del NP_009147.3:p.Leu361SerfsTer?
NM_181507.1:c.1423del , LRG_586t1:c.1423del NP_852608.1:p.Leu475SerfsTer?
NM_181508.1:c.1081del NP_852609.1:p.Leu361SerfsTer?
XM_011519862.1:c.1423del XP_011518164.1:p.Leu475SerfsTer?
XM_011519863.1:c.1423del XP_011518165.1:p.Leu475SerfsTer?
XM_011519864.1:c.1423del XP_011518166.1:p.Leu475SerfsTer?
XM_011519865.1:c.1312del XP_011518167.1:p.Leu438SerfsTer?
XM_011519866.1:c.1081del XP_011518168.1:p.Leu361SerfsTer?
XM_011519867.1:c.1081del XP_011518169.1:p.Leu361SerfsTer?
XM_011519868.1:c.1081del XP_011518170.1:p.Leu361SerfsTer?
XM_011519869.1:c.1423del XP_011518171.1:p.Leu475SerfsTer?
XM_011519870.1:c.1423del XP_011518172.1:p.Leu475SerfsTer?
XM_011519871.1:c.1423del XP_011518173.1:p.Leu475SerfsTer?
XM_011519868.3:c.1081del XP_011518170.1:p.Leu361SerfsTer?
XM_017017149.1:c.1423del XP_016872638.1:p.Leu475SerfsTer?
XM_017017150.1:c.1423del XP_016872639.1:p.Leu475SerfsTer?
XM_017017151.2:c.1312del XP_016872640.1:p.Leu438SerfsTer?
XM_017017152.1:c.1312del XP_016872641.1:p.Leu438SerfsTer?
XM_017017153.2:c.1312del XP_016872642.1:p.Leu438SerfsTer?
XM_017017154.1:c.1081del XP_016872643.1:p.Leu361SerfsTer?
XR_001747750.1:n.1692del
XR_001747751.1:n.1692del
XR_001747752.1:n.1448del
XR_001747753.1:n.1565del
XR_001747754.2:n.1667del
XR_001747755.2:n.1667del
XR_001747756.2:n.1680del
NM_007216.4:c.1081del NP_009147.3:p.Leu361SerfsTer?
NM_181507.2:c.1423del MANE Select NP_852608.1:p.Leu475SerfsTer?