Canonical Allele Identifier: CA379514903
Gene: HPS5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18285386T>A , CM000673.2:g.18285386T>A GRCh38
NC_000011.9:g.18306933T>A , CM000673.1:g.18306933T>A GRCh37
NC_000011.8:g.18263509T>A NCBI36
NG_008877.1:g.41789A>T , LRG_586:g.41789A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000349215.8:c.2911A>T MANE Select ENSP00000265967.5:p.Ile971Leu
ENST00000349215.7:c.2911A>T ENSP00000265967.5:p.Ile971Leu
ENST00000352460.7:n.1228+1205A>T
ENST00000396253.7:c.2569A>T ENSP00000379552.3:p.Ile857Leu
ENST00000438420.6:c.2569A>T ENSP00000399590.2:p.Ile857Leu
ENST00000537258.1:c.232A>T ENSP00000437437.1:p.Ile78Leu
ENST00000544218.5:c.469A>T ENSP00000441781.1:p.Ile157Leu
ENST00000545561.1:n.972A>T
NM_007216.3:c.2569A>T NP_009147.3:p.Ile857Leu
NM_181507.1:c.2911A>T , LRG_586t1:c.2911A>T NP_852608.1:p.Ile971Leu
NM_181508.1:c.2569A>T NP_852609.1:p.Ile857Leu
XM_011519862.1:c.2911A>T XP_011518164.1:p.Ile971Leu
XM_011519863.1:c.2911A>T XP_011518165.1:p.Ile971Leu
XM_011519864.1:c.2911A>T XP_011518166.1:p.Ile971Leu
XM_011519865.1:c.2800A>T XP_011518167.1:p.Ile934Leu
XM_011519866.1:c.2569A>T XP_011518168.1:p.Ile857Leu
XM_011519867.1:c.2569A>T XP_011518169.1:p.Ile857Leu
XM_011519868.1:c.2569A>T XP_011518170.1:p.Ile857Leu
XM_011519869.1:c.2911A>T XP_011518171.1:p.Ile971Leu
XM_011519868.3:c.2569A>T XP_011518170.1:p.Ile857Leu
XM_017017149.1:c.2911A>T XP_016872638.1:p.Ile971Leu
XM_017017150.1:c.2911A>T XP_016872639.1:p.Ile971Leu
XM_017017151.2:c.2800A>T XP_016872640.1:p.Ile934Leu
XM_017017152.1:c.2800A>T XP_016872641.1:p.Ile934Leu
XM_017017153.2:c.2800A>T XP_016872642.1:p.Ile934Leu
XM_017017154.1:c.2569A>T XP_016872643.1:p.Ile857Leu
XR_001747750.1:n.3180A>T
XR_001747751.1:n.3180A>T
XR_001747752.1:n.2936A>T
XR_001747753.1:n.3053A>T
XR_001747754.2:n.2577A>T
XR_001747755.2:n.2499A>T
XR_001747756.2:n.2512A>T
NM_007216.4:c.2569A>T NP_009147.3:p.Ile857Leu
NM_181507.2:c.2911A>T MANE Select NP_852608.1:p.Ile971Leu