Canonical Allele Identifier: CA339849328

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557826A>T (hg19) ; chr1:g.40092154A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092154A>T , CM000663.2:g.40092154A>T	GRCh38
NC_000001.10:g.40557826A>T , CM000663.1:g.40557826A>T	GRCh37
NC_000001.9:g.40330413A>T	NCBI36
NG_009192.1:g.10317T>A , LRG_690:g.10317T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*89T>A	ENSP00000361865.5:n.*89T>A
ENST00000433473.8:c.250T>A	ENSP00000394863.4:p.Phe84Ile
ENST00000439754.6:c.253T>A	ENSP00000403207.2:p.Phe85Ile
ENST00000449045.7:c.125-2642T>A	ENSP00000392293.2:n.125-2642T>A
ENST00000526547.2:c.533T>A
ENST00000527311.7:c.234+244T>A	ENSP00000436695.3:n.234+244T>A
ENST00000530704.6:c.253T>A	ENSP00000431655.1:p.Phe85Ile
ENST00000641083.1:c.231T>A
ENST00000641236.1:n.490T>A
ENST00000641319.1:c.253T>A	ENSP00000493128.1:p.Phe85Ile
ENST00000641471.1:c.340T>A	ENSP00000493146.1:p.Phe114Ile
ENST00000641548.1:c.*105T>A	ENSP00000492984.1:n.*105T>A
ENST00000641691.1:c.*105T>A	ENSP00000492910.1:n.*105T>A
ENST00000641924.1:c.124+4961T>A	ENSP00000493063.1:n.124+4961T>A
ENST00000642050.2:c.253T>A MANE Select	ENSP00000493153.1:p.Phe85Ile
ENST00000372779.8:c.340T>A	ENSP00000361865.4:p.Phe114Ile
ENST00000433473.7:c.253T>A	ENSP00000394863.3:p.Phe85Ile
ENST00000449045.6:c.125-2642T>A	ENSP00000392293.2:n.125-2642T>A
ENST00000526547.1:c.103T>A	ENSP00000436481.1:p.Phe35Ile
ENST00000527311.6:c.125-97T>A	ENSP00000436695.2:n.125-97T>A
ENST00000529905.5:c.253T>A	ENSP00000432053.1:p.Phe85Ile
ENST00000530704.5:c.253T>A	ENSP00000431655.1:p.Phe85Ile
NM_000310.3:c.253T>A , LRG_690t1:c.253T>A	NP_000301.1:p.Phe85Ile
NM_001142604.1:c.125-2642T>A	NP_001136076.1:n.125-2642T>A
XM_005271008.1:c.253T>A	XP_005271065.1:p.Phe85Ile
NM_001363695.1:c.253T>A	NP_001350624.1:p.Phe85Ile
NM_000310.4:c.253T>A MANE Select	NP_000301.1:p.Phe85Ile
NM_001142604.2:c.125-2642T>A	NP_001136076.1:n.125-2642T>A
NM_001363695.2:c.253T>A	NP_001350624.1:p.Phe85Ile