Canonical Allele Identifier: CA379518679

Gene: HPS5

Linked Data

• MyVariant Identifiers: chr11:g.18309115T>A (hg19) ; chr11:g.18287568T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18287568T>A , CM000673.2:g.18287568T>A	GRCh38
NC_000011.9:g.18309115T>A , CM000673.1:g.18309115T>A	GRCh37
NC_000011.8:g.18265691T>A	NCBI36
NG_008877.1:g.39607A>T , LRG_586:g.39607A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349215.8:c.2684A>T MANE Select	ENSP00000265967.5:p.Asp895Val
ENST00000349215.7:c.2684A>T	ENSP00000265967.5:p.Asp895Val
ENST00000352460.7:n.1075A>T
ENST00000396253.7:c.2342A>T	ENSP00000379552.3:p.Asp781Val
ENST00000438420.6:c.2342A>T	ENSP00000399590.2:p.Asp781Val
ENST00000544218.5:c.242A>T	ENSP00000441781.1:p.Asp81Val
ENST00000545561.1:n.745A>T
NM_007216.3:c.2342A>T	NP_009147.3:p.Asp781Val
NM_181507.1:c.2684A>T , LRG_586t1:c.2684A>T	NP_852608.1:p.Asp895Val
NM_181508.1:c.2342A>T	NP_852609.1:p.Asp781Val
XM_011519862.1:c.2684A>T	XP_011518164.1:p.Asp895Val
XM_011519863.1:c.2684A>T	XP_011518165.1:p.Asp895Val
XM_011519864.1:c.2684A>T	XP_011518166.1:p.Asp895Val
XM_011519865.1:c.2573A>T	XP_011518167.1:p.Asp858Val
XM_011519866.1:c.2342A>T	XP_011518168.1:p.Asp781Val
XM_011519867.1:c.2342A>T	XP_011518169.1:p.Asp781Val
XM_011519868.1:c.2342A>T	XP_011518170.1:p.Asp781Val
XM_011519869.1:c.2684A>T	XP_011518171.1:p.Asp895Val
XM_011519870.1:c.*168A>T	XP_011518172.1:n.*168A>T
XM_011519871.1:c.*168A>T	XP_011518173.1:n.*168A>T
XM_011519868.3:c.2342A>T	XP_011518170.1:p.Asp781Val
XM_017017149.1:c.2684A>T	XP_016872638.1:p.Asp895Val
XM_017017150.1:c.2684A>T	XP_016872639.1:p.Asp895Val
XM_017017151.2:c.2573A>T	XP_016872640.1:p.Asp858Val
XM_017017152.1:c.2573A>T	XP_016872641.1:p.Asp858Val
XM_017017153.2:c.2573A>T	XP_016872642.1:p.Asp858Val
XM_017017154.1:c.2342A>T	XP_016872643.1:p.Asp781Val
XR_001747750.1:n.2953A>T
XR_001747751.1:n.2953A>T
XR_001747752.1:n.2709A>T
XR_001747753.1:n.2826A>T
XR_001747754.2:n.2350A>T
XR_001747755.2:n.2272A>T
XR_001747756.2:n.2285A>T
NM_007216.4:c.2342A>T	NP_009147.3:p.Asp781Val
NM_181507.2:c.2684A>T MANE Select	NP_852608.1:p.Asp895Val