Canonical Allele Identifier: CA379491684

Gene: HPS5

Linked Data

• dbSNP Id: rs2134287934
• MyVariant Identifiers: chr11:g.18313566C>A (hg19) ; chr11:g.18292019C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18292019C>A , CM000673.2:g.18292019C>A	GRCh38
NC_000011.9:g.18313566C>A , CM000673.1:g.18313566C>A	GRCh37
NC_000011.8:g.18270142C>A	NCBI36
NG_008877.1:g.35156G>T , LRG_586:g.35156G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349215.8:c.1863G>T MANE Select	ENSP00000265967.5:p.Met621Ile
ENST00000349215.7:c.1863G>T	ENSP00000265967.5:p.Met621Ile
ENST00000352460.7:n.254G>T
ENST00000396253.7:c.1521G>T	ENSP00000379552.3:p.Met507Ile
ENST00000438420.6:c.1521G>T	ENSP00000399590.2:p.Met507Ile
ENST00000543728.1:n.197+3001G>T
ENST00000544218.5:c.-3+880G>T	ENSP00000441781.1:n.-3+880G>T
NM_007216.3:c.1521G>T	NP_009147.3:p.Met507Ile
NM_181507.1:c.1863G>T , LRG_586t1:c.1863G>T	NP_852608.1:p.Met621Ile
NM_181508.1:c.1521G>T	NP_852609.1:p.Met507Ile
XM_011519862.1:c.1863G>T	XP_011518164.1:p.Met621Ile
XM_011519863.1:c.1863G>T	XP_011518165.1:p.Met621Ile
XM_011519864.1:c.1863G>T	XP_011518166.1:p.Met621Ile
XM_011519865.1:c.1752G>T	XP_011518167.1:p.Met584Ile
XM_011519866.1:c.1521G>T	XP_011518168.1:p.Met507Ile
XM_011519867.1:c.1521G>T	XP_011518169.1:p.Met507Ile
XM_011519868.1:c.1521G>T	XP_011518170.1:p.Met507Ile
XM_011519869.1:c.1863G>T	XP_011518171.1:p.Met621Ile
XM_011519870.1:c.1862+880G>T	XP_011518172.1:n.1862+880G>T
XM_011519871.1:c.1784+3001G>T	XP_011518173.1:n.1784+3001G>T
XM_011519868.3:c.1521G>T	XP_011518170.1:p.Met507Ile
XM_017017149.1:c.1863G>T	XP_016872638.1:p.Met621Ile
XM_017017150.1:c.1863G>T	XP_016872639.1:p.Met621Ile
XM_017017151.2:c.1752G>T	XP_016872640.1:p.Met584Ile
XM_017017152.1:c.1752G>T	XP_016872641.1:p.Met584Ile
XM_017017153.2:c.1752G>T	XP_016872642.1:p.Met584Ile
XM_017017154.1:c.1521G>T	XP_016872643.1:p.Met507Ile
XR_001747750.1:n.2132G>T
XR_001747751.1:n.2132G>T
XR_001747752.1:n.1888G>T
XR_001747753.1:n.2005G>T
XR_001747754.2:n.2106+880G>T
XR_001747755.2:n.2028+3001G>T
XR_001747756.2:n.2041+3001G>T
NM_007216.4:c.1521G>T	NP_009147.3:p.Met507Ile
NM_181507.2:c.1863G>T MANE Select	NP_852608.1:p.Met621Ile