Canonical Allele Identifier: CA379518776

Gene: HPS5

Linked Data

• MyVariant Identifiers: chr11:g.18309130A>T (hg19) ; chr11:g.18287583A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18287583A>T , CM000673.2:g.18287583A>T	GRCh38
NC_000011.9:g.18309130A>T , CM000673.1:g.18309130A>T	GRCh37
NC_000011.8:g.18265706A>T	NCBI36
NG_008877.1:g.39592T>A , LRG_586:g.39592T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349215.8:c.2669T>A MANE Select	ENSP00000265967.5:p.Phe890Tyr
ENST00000349215.7:c.2669T>A	ENSP00000265967.5:p.Phe890Tyr
ENST00000352460.7:n.1060T>A
ENST00000396253.7:c.2327T>A	ENSP00000379552.3:p.Phe776Tyr
ENST00000438420.6:c.2327T>A	ENSP00000399590.2:p.Phe776Tyr
ENST00000544218.5:c.227T>A	ENSP00000441781.1:p.Phe76Tyr
ENST00000545561.1:n.730T>A
NM_007216.3:c.2327T>A	NP_009147.3:p.Phe776Tyr
NM_181507.1:c.2669T>A , LRG_586t1:c.2669T>A	NP_852608.1:p.Phe890Tyr
NM_181508.1:c.2327T>A	NP_852609.1:p.Phe776Tyr
XM_011519862.1:c.2669T>A	XP_011518164.1:p.Phe890Tyr
XM_011519863.1:c.2669T>A	XP_011518165.1:p.Phe890Tyr
XM_011519864.1:c.2669T>A	XP_011518166.1:p.Phe890Tyr
XM_011519865.1:c.2558T>A	XP_011518167.1:p.Phe853Tyr
XM_011519866.1:c.2327T>A	XP_011518168.1:p.Phe776Tyr
XM_011519867.1:c.2327T>A	XP_011518169.1:p.Phe776Tyr
XM_011519868.1:c.2327T>A	XP_011518170.1:p.Phe776Tyr
XM_011519869.1:c.2669T>A	XP_011518171.1:p.Phe890Tyr
XM_011519870.1:c.*153T>A	XP_011518172.1:n.*153T>A
XM_011519871.1:c.*153T>A	XP_011518173.1:n.*153T>A
XM_011519868.3:c.2327T>A	XP_011518170.1:p.Phe776Tyr
XM_017017149.1:c.2669T>A	XP_016872638.1:p.Phe890Tyr
XM_017017150.1:c.2669T>A	XP_016872639.1:p.Phe890Tyr
XM_017017151.2:c.2558T>A	XP_016872640.1:p.Phe853Tyr
XM_017017152.1:c.2558T>A	XP_016872641.1:p.Phe853Tyr
XM_017017153.2:c.2558T>A	XP_016872642.1:p.Phe853Tyr
XM_017017154.1:c.2327T>A	XP_016872643.1:p.Phe776Tyr
XR_001747750.1:n.2938T>A
XR_001747751.1:n.2938T>A
XR_001747752.1:n.2694T>A
XR_001747753.1:n.2811T>A
XR_001747754.2:n.2335T>A
XR_001747755.2:n.2257T>A
XR_001747756.2:n.2270T>A
NM_007216.4:c.2327T>A	NP_009147.3:p.Phe776Tyr
NM_181507.2:c.2669T>A MANE Select	NP_852608.1:p.Phe890Tyr