Canonical Allele Identifier: CA918829248

Gene: HPS5

Linked Data

• dbSNP Id: rs1590059699

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18287508_18287509del , CM000673.2:g.18287508_18287509del	GRCh38
NC_000011.9:g.18309055_18309056del , CM000673.1:g.18309055_18309056del	GRCh37
NC_000011.8:g.18265631_18265632del	NCBI36
NG_008877.1:g.39669_39670del , LRG_586:g.39669_39670del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349215.8:c.2717+29_2717+30del MANE Select	ENSP00000265967.5:n.2717+29_2717+30del
ENST00000349215.7:c.2717+29_2717+30del	ENSP00000265967.5:n.2717+29_2717+30del
ENST00000352460.7:n.1108+29_1108+30del
ENST00000396253.7:c.2375+29_2375+30del	ENSP00000379552.3:n.2375+29_2375+30del
ENST00000438420.6:c.2375+29_2375+30del	ENSP00000399590.2:n.2375+29_2375+30del
ENST00000544218.5:c.275+29_275+30del	ENSP00000441781.1:n.275+29_275+30del
ENST00000545561.1:n.778+29_778+30del
NM_007216.3:c.2375+29_2375+30del	NP_009147.3:n.2375+29_2375+30del
NM_181507.1:c.2717+29_2717+30del , LRG_586t1:c.2717+29_2717+30del	NP_852608.1:n.2717+29_2717+30del
NM_181508.1:c.2375+29_2375+30del	NP_852609.1:n.2375+29_2375+30del
XM_011519862.1:c.2717+29_2717+30del	XP_011518164.1:n.2717+29_2717+30del
XM_011519863.1:c.2717+29_2717+30del	XP_011518165.1:n.2717+29_2717+30del
XM_011519864.1:c.2717+29_2717+30del	XP_011518166.1:n.2717+29_2717+30del
XM_011519865.1:c.2606+29_2606+30del	XP_011518167.1:n.2606+29_2606+30del
XM_011519866.1:c.2375+29_2375+30del	XP_011518168.1:n.2375+29_2375+30del
XM_011519867.1:c.2375+29_2375+30del	XP_011518169.1:n.2375+29_2375+30del
XM_011519868.1:c.2375+29_2375+30del	XP_011518170.1:n.2375+29_2375+30del
XM_011519869.1:c.2717+29_2717+30del	XP_011518171.1:n.2717+29_2717+30del
XM_011519868.3:c.2375+29_2375+30del	XP_011518170.1:n.2375+29_2375+30del
XM_017017149.1:c.2717+29_2717+30del	XP_016872638.1:n.2717+29_2717+30del
XM_017017150.1:c.2717+29_2717+30del	XP_016872639.1:n.2717+29_2717+30del
XM_017017151.2:c.2606+29_2606+30del	XP_016872640.1:n.2606+29_2606+30del
XM_017017152.1:c.2606+29_2606+30del	XP_016872641.1:n.2606+29_2606+30del
XM_017017153.2:c.2606+29_2606+30del	XP_016872642.1:n.2606+29_2606+30del
XM_017017154.1:c.2375+29_2375+30del	XP_016872643.1:n.2375+29_2375+30del
XR_001747750.1:n.2986+29_2986+30del
XR_001747751.1:n.2986+29_2986+30del
XR_001747752.1:n.2742+29_2742+30del
XR_001747753.1:n.2859+29_2859+30del
XR_001747754.2:n.2383+29_2383+30del
XR_001747755.2:n.2305+29_2305+30del
XR_001747756.2:n.2318+29_2318+30del
NM_007216.4:c.2375+29_2375+30del	NP_009147.3:n.2375+29_2375+30del
NM_181507.2:c.2717+29_2717+30del MANE Select	NP_852608.1:n.2717+29_2717+30del