Canonical Allele Identifier: CA379518880

Gene: HPS5

Linked Data

• MyVariant Identifiers: chr11:g.18309146G>C (hg19) ; chr11:g.18287599G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18287599G>C , CM000673.2:g.18287599G>C	GRCh38
NC_000011.9:g.18309146G>C , CM000673.1:g.18309146G>C	GRCh37
NC_000011.8:g.18265722G>C	NCBI36
NG_008877.1:g.39576C>G , LRG_586:g.39576C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349215.8:c.2653C>G MANE Select	ENSP00000265967.5:p.His885Asp
ENST00000349215.7:c.2653C>G	ENSP00000265967.5:p.His885Asp
ENST00000352460.7:n.1044C>G
ENST00000396253.7:c.2311C>G	ENSP00000379552.3:p.His771Asp
ENST00000438420.6:c.2311C>G	ENSP00000399590.2:p.His771Asp
ENST00000544218.5:c.211C>G	ENSP00000441781.1:p.His71Asp
ENST00000545561.1:n.714C>G
NM_007216.3:c.2311C>G	NP_009147.3:p.His771Asp
NM_181507.1:c.2653C>G , LRG_586t1:c.2653C>G	NP_852608.1:p.His885Asp
NM_181508.1:c.2311C>G	NP_852609.1:p.His771Asp
XM_011519862.1:c.2653C>G	XP_011518164.1:p.His885Asp
XM_011519863.1:c.2653C>G	XP_011518165.1:p.His885Asp
XM_011519864.1:c.2653C>G	XP_011518166.1:p.His885Asp
XM_011519865.1:c.2542C>G	XP_011518167.1:p.His848Asp
XM_011519866.1:c.2311C>G	XP_011518168.1:p.His771Asp
XM_011519867.1:c.2311C>G	XP_011518169.1:p.His771Asp
XM_011519868.1:c.2311C>G	XP_011518170.1:p.His771Asp
XM_011519869.1:c.2653C>G	XP_011518171.1:p.His885Asp
XM_011519870.1:c.*137C>G	XP_011518172.1:n.*137C>G
XM_011519871.1:c.*137C>G	XP_011518173.1:n.*137C>G
XM_011519868.3:c.2311C>G	XP_011518170.1:p.His771Asp
XM_017017149.1:c.2653C>G	XP_016872638.1:p.His885Asp
XM_017017150.1:c.2653C>G	XP_016872639.1:p.His885Asp
XM_017017151.2:c.2542C>G	XP_016872640.1:p.His848Asp
XM_017017152.1:c.2542C>G	XP_016872641.1:p.His848Asp
XM_017017153.2:c.2542C>G	XP_016872642.1:p.His848Asp
XM_017017154.1:c.2311C>G	XP_016872643.1:p.His771Asp
XR_001747750.1:n.2922C>G
XR_001747751.1:n.2922C>G
XR_001747752.1:n.2678C>G
XR_001747753.1:n.2795C>G
XR_001747754.2:n.2319C>G
XR_001747755.2:n.2241C>G
XR_001747756.2:n.2254C>G
NM_007216.4:c.2311C>G	NP_009147.3:p.His771Asp
NM_181507.2:c.2653C>G MANE Select	NP_852608.1:p.His885Asp