Canonical Allele Identifier: CA473371561

Gene: HPS5

Linked Data

• ClinVar Variation Id: 2836215
• ClinVar RCV Id: RCV003689967
• MyVariant Identifiers: chr11:g.18309210A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18287663A>G , CM000673.2:g.18287663A>G	GRCh38
NC_000011.9:g.18309210A>G , CM000673.1:g.18309210A>G	GRCh37
NC_000011.8:g.18265786A>G	NCBI36
NG_008877.1:g.39512T>C , LRG_586:g.39512T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000349215.8:c.2589T>C MANE Select	ENSP00000265967.5:p.Ala863=
ENST00000349215.7:c.2589T>C	ENSP00000265967.5:p.Ala863=
ENST00000352460.7:n.980T>C
ENST00000396253.7:c.2247T>C	ENSP00000379552.3:p.Ala749=
ENST00000438420.6:c.2247T>C	ENSP00000399590.2:p.Ala749=
ENST00000544218.5:c.147T>C	ENSP00000441781.1:p.Ala49=
ENST00000545561.1:n.650T>C
NM_007216.3:c.2247T>C	NP_009147.3:p.Ala749=
NM_181507.1:c.2589T>C , LRG_586t1:c.2589T>C	NP_852608.1:p.Ala863=
NM_181508.1:c.2247T>C	NP_852609.1:p.Ala749=
XM_011519862.1:c.2589T>C	XP_011518164.1:p.Ala863=
XM_011519863.1:c.2589T>C	XP_011518165.1:p.Ala863=
XM_011519864.1:c.2589T>C	XP_011518166.1:p.Ala863=
XM_011519865.1:c.2478T>C	XP_011518167.1:p.Ala826=
XM_011519866.1:c.2247T>C	XP_011518168.1:p.Ala749=
XM_011519867.1:c.2247T>C	XP_011518169.1:p.Ala749=
XM_011519868.1:c.2247T>C	XP_011518170.1:p.Ala749=
XM_011519869.1:c.2589T>C	XP_011518171.1:p.Ala863=
XM_011519870.1:c.*73T>C	XP_011518172.1:n.*73T>C
XM_011519871.1:c.*73T>C	XP_011518173.1:n.*73T>C
XM_011519868.3:c.2247T>C	XP_011518170.1:p.Ala749=
XM_017017149.1:c.2589T>C	XP_016872638.1:p.Ala863=
XM_017017150.1:c.2589T>C	XP_016872639.1:p.Ala863=
XM_017017151.2:c.2478T>C	XP_016872640.1:p.Ala826=
XM_017017152.1:c.2478T>C	XP_016872641.1:p.Ala826=
XM_017017153.2:c.2478T>C	XP_016872642.1:p.Ala826=
XM_017017154.1:c.2247T>C	XP_016872643.1:p.Ala749=
XR_001747750.1:n.2858T>C
XR_001747751.1:n.2858T>C
XR_001747752.1:n.2614T>C
XR_001747753.1:n.2731T>C
XR_001747754.2:n.2255T>C
XR_001747755.2:n.2177T>C
XR_001747756.2:n.2190T>C
NM_007216.4:c.2247T>C	NP_009147.3:p.Ala749=
NM_181507.2:c.2589T>C MANE Select	NP_852608.1:p.Ala863=