Canonical Allele Identifier: CA1955516233
Gene: HPS5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18287540A= , CM000673.2:g.18287540A= GRCh38
NC_000011.9:g.18309087A= , CM000673.1:g.18309087A= GRCh37
NC_000011.8:g.18265663A= NCBI36
NG_008877.1:g.39635T= , LRG_586:g.39635T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000349215.8:c.2712T= MANE Select ENSP00000265967.5:p.Asp904=
ENST00000349215.7:c.2712T= ENSP00000265967.5:p.Asp904=
ENST00000352460.7:n.1103T=
ENST00000396253.7:c.2370T= ENSP00000379552.3:p.Asp790=
ENST00000438420.6:c.2370T= ENSP00000399590.2:p.Asp790=
ENST00000544218.5:c.270T= ENSP00000441781.1:p.Asp90=
ENST00000545561.1:n.773T=
NM_007216.3:c.2370T= NP_009147.3:p.Asp790=
NM_181507.1:c.2712T= , LRG_586t1:c.2712T= NP_852608.1:p.Asp904=
NM_181508.1:c.2370T= NP_852609.1:p.Asp790=
XM_011519862.1:c.2712T= XP_011518164.1:p.Asp904=
XM_011519863.1:c.2712T= XP_011518165.1:p.Asp904=
XM_011519864.1:c.2712T= XP_011518166.1:p.Asp904=
XM_011519865.1:c.2601T= XP_011518167.1:p.Asp867=
XM_011519866.1:c.2370T= XP_011518168.1:p.Asp790=
XM_011519867.1:c.2370T= XP_011518169.1:p.Asp790=
XM_011519868.1:c.2370T= XP_011518170.1:p.Asp790=
XM_011519869.1:c.2712T= XP_011518171.1:p.Asp904=
XM_011519868.3:c.2370T= XP_011518170.1:p.Asp790=
XM_017017149.1:c.2712T= XP_016872638.1:p.Asp904=
XM_017017150.1:c.2712T= XP_016872639.1:p.Asp904=
XM_017017151.2:c.2601T= XP_016872640.1:p.Asp867=
XM_017017152.1:c.2601T= XP_016872641.1:p.Asp867=
XM_017017153.2:c.2601T= XP_016872642.1:p.Asp867=
XM_017017154.1:c.2370T= XP_016872643.1:p.Asp790=
XR_001747750.1:n.2981T=
XR_001747751.1:n.2981T=
XR_001747752.1:n.2737T=
XR_001747753.1:n.2854T=
XR_001747754.2:n.2378T=
XR_001747755.2:n.2300T=
XR_001747756.2:n.2313T=
NM_007216.4:c.2370T= NP_009147.3:p.Asp790=
NM_181507.2:c.2712T= MANE Select NP_852608.1:p.Asp904=