Canonical Allele Identifier: CA354921993

Gene: HPS3

Linked Data

• MyVariant Identifiers: chr3:g.148875280T>A (hg19) ; chr3:g.149157493T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149157493T>A , CM000665.2:g.149157493T>A	GRCh38
NC_000003.11:g.148875280T>A , CM000665.1:g.148875280T>A	GRCh37
NC_000003.10:g.150357970T>A	NCBI36
NG_009847.1:g.32910T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296051.7:c.1653T>A MANE Select	ENSP00000296051.2:p.Phe551Leu
ENST00000296051.6:c.1653T>A	ENSP00000296051.2:p.Phe551Leu
ENST00000460120.5:c.1158T>A	ENSP00000418230.1:p.Phe386Leu
NM_001308258.1:c.1158T>A	NP_001295187.1:p.Phe386Leu
NM_032383.3:c.1653T>A	NP_115759.2:p.Phe551Leu
NM_032383.4:c.1653T>A	NP_115759.2:p.Phe551Leu
XM_005247834.3:c.1653T>A	XP_005247891.1:p.Phe551Leu
XM_006713788.1:c.1653T>A	XP_006713851.1:p.Phe551Leu
XR_924201.1:n.1768T>A
XM_005247834.4:c.1653T>A	XP_005247891.1:p.Phe551Leu
XM_017007323.2:c.1653T>A	XP_016862812.1:p.Phe551Leu
XR_001740326.2:n.1753T>A
XR_001740327.2:n.1753T>A
XR_001740328.2:n.1753T>A
XR_924201.3:n.1753T>A
NM_001308258.2:c.1158T>A	NP_001295187.1:p.Phe386Leu
NM_032383.5:c.1653T>A MANE Select	NP_115759.2:p.Phe551Leu