Canonical Allele Identifier: CA674316571

Gene: HPS5

Linked Data

• dbSNP Id: rs1395520471
• gnomAD v3: 11-18292028-G-A
• gnomAD v4: 11-18292028-G-A
• MyVariant Identifiers: chr11:g.18313575G>A (hg19) ; chr11:g.18292028G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18292028G>A , CM000673.2:g.18292028G>A	GRCh38
NC_000011.9:g.18313575G>A , CM000673.1:g.18313575G>A	GRCh37
NC_000011.8:g.18270151G>A	NCBI36
NG_008877.1:g.35147C>T , LRG_586:g.35147C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349215.8:c.1863-9C>T MANE Select	ENSP00000265967.5:n.1863-9C>T
ENST00000349215.7:c.1863-9C>T	ENSP00000265967.5:n.1863-9C>T
ENST00000352460.7:n.254-9C>T
ENST00000396253.7:c.1521-9C>T	ENSP00000379552.3:n.1521-9C>T
ENST00000438420.6:c.1521-9C>T	ENSP00000399590.2:n.1521-9C>T
ENST00000543728.1:n.197+2992C>T
ENST00000544218.5:c.-3+871C>T	ENSP00000441781.1:n.-3+871C>T
NM_007216.3:c.1521-9C>T	NP_009147.3:n.1521-9C>T
NM_181507.1:c.1863-9C>T , LRG_586t1:c.1863-9C>T	NP_852608.1:n.1863-9C>T
NM_181508.1:c.1521-9C>T	NP_852609.1:n.1521-9C>T
XM_011519862.1:c.1863-9C>T	XP_011518164.1:n.1863-9C>T
XM_011519863.1:c.1863-9C>T	XP_011518165.1:n.1863-9C>T
XM_011519864.1:c.1863-9C>T	XP_011518166.1:n.1863-9C>T
XM_011519865.1:c.1752-9C>T	XP_011518167.1:n.1752-9C>T
XM_011519866.1:c.1521-9C>T	XP_011518168.1:n.1521-9C>T
XM_011519867.1:c.1521-9C>T	XP_011518169.1:n.1521-9C>T
XM_011519868.1:c.1521-9C>T	XP_011518170.1:n.1521-9C>T
XM_011519869.1:c.1863-9C>T	XP_011518171.1:n.1863-9C>T
XM_011519870.1:c.1862+871C>T	XP_011518172.1:n.1862+871C>T
XM_011519871.1:c.1784+2992C>T	XP_011518173.1:n.1784+2992C>T
XM_011519868.3:c.1521-9C>T	XP_011518170.1:n.1521-9C>T
XM_017017149.1:c.1863-9C>T	XP_016872638.1:n.1863-9C>T
XM_017017150.1:c.1863-9C>T	XP_016872639.1:n.1863-9C>T
XM_017017151.2:c.1752-9C>T	XP_016872640.1:n.1752-9C>T
XM_017017152.1:c.1752-9C>T	XP_016872641.1:n.1752-9C>T
XM_017017153.2:c.1752-9C>T	XP_016872642.1:n.1752-9C>T
XM_017017154.1:c.1521-9C>T	XP_016872643.1:n.1521-9C>T
XR_001747750.1:n.2132-9C>T
XR_001747751.1:n.2132-9C>T
XR_001747752.1:n.1888-9C>T
XR_001747753.1:n.2005-9C>T
XR_001747754.2:n.2106+871C>T
XR_001747755.2:n.2028+2992C>T
XR_001747756.2:n.2041+2992C>T
NM_007216.4:c.1521-9C>T	NP_009147.3:n.1521-9C>T
NM_181507.2:c.1863-9C>T MANE Select	NP_852608.1:n.1863-9C>T