Canonical Allele Identifier: CA379518515

Gene: HPS5

Linked Data

• MyVariant Identifiers: chr11:g.18309088T>A (hg19) ; chr11:g.18287541T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18287541T>A , CM000673.2:g.18287541T>A	GRCh38
NC_000011.9:g.18309088T>A , CM000673.1:g.18309088T>A	GRCh37
NC_000011.8:g.18265664T>A	NCBI36
NG_008877.1:g.39634A>T , LRG_586:g.39634A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000349215.8:c.2711A>T MANE Select	ENSP00000265967.5:p.Asp904Val
ENST00000349215.7:c.2711A>T	ENSP00000265967.5:p.Asp904Val
ENST00000352460.7:n.1102A>T
ENST00000396253.7:c.2369A>T	ENSP00000379552.3:p.Asp790Val
ENST00000438420.6:c.2369A>T	ENSP00000399590.2:p.Asp790Val
ENST00000544218.5:c.269A>T	ENSP00000441781.1:p.Asp90Val
ENST00000545561.1:n.772A>T
NM_007216.3:c.2369A>T	NP_009147.3:p.Asp790Val
NM_181507.1:c.2711A>T , LRG_586t1:c.2711A>T	NP_852608.1:p.Asp904Val
NM_181508.1:c.2369A>T	NP_852609.1:p.Asp790Val
XM_011519862.1:c.2711A>T	XP_011518164.1:p.Asp904Val
XM_011519863.1:c.2711A>T	XP_011518165.1:p.Asp904Val
XM_011519864.1:c.2711A>T	XP_011518166.1:p.Asp904Val
XM_011519865.1:c.2600A>T	XP_011518167.1:p.Asp867Val
XM_011519866.1:c.2369A>T	XP_011518168.1:p.Asp790Val
XM_011519867.1:c.2369A>T	XP_011518169.1:p.Asp790Val
XM_011519868.1:c.2369A>T	XP_011518170.1:p.Asp790Val
XM_011519869.1:c.2711A>T	XP_011518171.1:p.Asp904Val
XM_011519868.3:c.2369A>T	XP_011518170.1:p.Asp790Val
XM_017017149.1:c.2711A>T	XP_016872638.1:p.Asp904Val
XM_017017150.1:c.2711A>T	XP_016872639.1:p.Asp904Val
XM_017017151.2:c.2600A>T	XP_016872640.1:p.Asp867Val
XM_017017152.1:c.2600A>T	XP_016872641.1:p.Asp867Val
XM_017017153.2:c.2600A>T	XP_016872642.1:p.Asp867Val
XM_017017154.1:c.2369A>T	XP_016872643.1:p.Asp790Val
XR_001747750.1:n.2980A>T
XR_001747751.1:n.2980A>T
XR_001747752.1:n.2736A>T
XR_001747753.1:n.2853A>T
XR_001747754.2:n.2377A>T
XR_001747755.2:n.2299A>T
XR_001747756.2:n.2312A>T
NM_007216.4:c.2369A>T	NP_009147.3:p.Asp790Val
NM_181507.2:c.2711A>T MANE Select	NP_852608.1:p.Asp904Val