Canonical Allele Identifier: CA379514927
Gene: HPS5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18285388A>T , CM000673.2:g.18285388A>T GRCh38
NC_000011.9:g.18306935A>T , CM000673.1:g.18306935A>T GRCh37
NC_000011.8:g.18263511A>T NCBI36
NG_008877.1:g.41787T>A , LRG_586:g.41787T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000349215.8:c.2909T>A MANE Select ENSP00000265967.5:p.Phe970Tyr
ENST00000349215.7:c.2909T>A ENSP00000265967.5:p.Phe970Tyr
ENST00000352460.7:n.1228+1203T>A
ENST00000396253.7:c.2567T>A ENSP00000379552.3:p.Phe856Tyr
ENST00000438420.6:c.2567T>A ENSP00000399590.2:p.Phe856Tyr
ENST00000537258.1:c.230T>A ENSP00000437437.1:p.Phe77Tyr
ENST00000544218.5:c.467T>A ENSP00000441781.1:p.Phe156Tyr
ENST00000545561.1:n.970T>A
NM_007216.3:c.2567T>A NP_009147.3:p.Phe856Tyr
NM_181507.1:c.2909T>A , LRG_586t1:c.2909T>A NP_852608.1:p.Phe970Tyr
NM_181508.1:c.2567T>A NP_852609.1:p.Phe856Tyr
XM_011519862.1:c.2909T>A XP_011518164.1:p.Phe970Tyr
XM_011519863.1:c.2909T>A XP_011518165.1:p.Phe970Tyr
XM_011519864.1:c.2909T>A XP_011518166.1:p.Phe970Tyr
XM_011519865.1:c.2798T>A XP_011518167.1:p.Phe933Tyr
XM_011519866.1:c.2567T>A XP_011518168.1:p.Phe856Tyr
XM_011519867.1:c.2567T>A XP_011518169.1:p.Phe856Tyr
XM_011519868.1:c.2567T>A XP_011518170.1:p.Phe856Tyr
XM_011519869.1:c.2909T>A XP_011518171.1:p.Phe970Tyr
XM_011519868.3:c.2567T>A XP_011518170.1:p.Phe856Tyr
XM_017017149.1:c.2909T>A XP_016872638.1:p.Phe970Tyr
XM_017017150.1:c.2909T>A XP_016872639.1:p.Phe970Tyr
XM_017017151.2:c.2798T>A XP_016872640.1:p.Phe933Tyr
XM_017017152.1:c.2798T>A XP_016872641.1:p.Phe933Tyr
XM_017017153.2:c.2798T>A XP_016872642.1:p.Phe933Tyr
XM_017017154.1:c.2567T>A XP_016872643.1:p.Phe856Tyr
XR_001747750.1:n.3178T>A
XR_001747751.1:n.3178T>A
XR_001747752.1:n.2934T>A
XR_001747753.1:n.3051T>A
XR_001747754.2:n.2575T>A
XR_001747755.2:n.2497T>A
XR_001747756.2:n.2510T>A
NM_007216.4:c.2567T>A NP_009147.3:p.Phe856Tyr
NM_181507.2:c.2909T>A MANE Select NP_852608.1:p.Phe970Tyr