Canonical Allele Identifier: CA1955529771

Gene: HPS5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18281986G= , CM000673.2:g.18281986G=	GRCh38
NC_000011.9:g.18303533G= , CM000673.1:g.18303533G=	GRCh37
NC_000011.8:g.18260109G=	NCBI36
NG_008877.1:g.45189C= , LRG_586:g.45189C=

Transcript Alleles

HGVS	Amino-acid Change
NM_181507.2:c.3293C= MANE Select	NP_852608.1:p.Thr1098=
ENST00000349215.8:c.3293C= MANE Select	ENSP00000265967.5:p.Thr1098=
NM_007216.3:c.2951C=	NP_009147.3:p.Thr984=
NM_007216.4:c.2951C=	NP_009147.3:p.Thr984=
NM_181507.1:c.3293C= , LRG_586t1:c.3293C=	NP_852608.1:p.Thr1098=
NM_181508.1:c.2951C=	NP_852609.1:p.Thr984=
ENST00000349215.7:c.3293C=	ENSP00000265967.5:p.Thr1098=
ENST00000352460.7:n.1570C=
ENST00000396253.7:c.2951C=	ENSP00000379552.3:p.Thr984=
ENST00000438420.6:c.2951C=	ENSP00000399590.2:p.Thr984=
ENST00000537258.1:c.614C=	ENSP00000437437.1:p.Thr205=
XM_011519862.1:c.3293C=	XP_011518164.1:p.Thr1098=
XM_011519863.1:c.3293C=	XP_011518165.1:p.Thr1098=
XM_011519864.1:c.3293C=	XP_011518166.1:p.Thr1098=
XM_011519865.1:c.3182C=	XP_011518167.1:p.Thr1061=
XM_011519866.1:c.2951C=	XP_011518168.1:p.Thr984=
XM_011519867.1:c.2951C=	XP_011518169.1:p.Thr984=
XM_011519868.1:c.2951C=	XP_011518170.1:p.Thr984=
XM_011519868.3:c.2951C=	XP_011518170.1:p.Thr984=
XM_017017149.1:c.3293C=	XP_016872638.1:p.Thr1098=
XM_017017150.1:c.3293C=	XP_016872639.1:p.Thr1098=
XM_017017151.2:c.3182C=	XP_016872640.1:p.Thr1061=
XM_017017152.1:c.3182C=	XP_016872641.1:p.Thr1061=
XM_017017153.2:c.3182C=	XP_016872642.1:p.Thr1061=
XM_017017154.1:c.2951C=	XP_016872643.1:p.Thr984=
XR_001747750.1:n.3455C=
XR_001747751.1:n.3622C=
XR_001747752.1:n.3211C=
XR_001747753.1:n.3328C=
XR_001747754.2:n.2959C=
XR_001747755.2:n.2881C=
XR_001747756.2:n.2954C=