Canonical Allele Identifier: CA339849154

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557781C>T (hg19) ; chr1:g.40092109C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092109C>T , CM000663.2:g.40092109C>T	GRCh38
NC_000001.10:g.40557781C>T , CM000663.1:g.40557781C>T	GRCh37
NC_000001.9:g.40330368C>T	NCBI36
NG_009192.1:g.10362G>A , LRG_690:g.10362G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*134G>A	ENSP00000361865.5:n.*134G>A
ENST00000433473.8:c.295G>A	ENSP00000394863.4:p.Ala99Thr
ENST00000439754.6:c.298G>A	ENSP00000403207.2:p.Ala100Thr
ENST00000449045.7:c.125-2597G>A	ENSP00000392293.2:n.125-2597G>A
ENST00000526547.2:c.578G>A
ENST00000527311.7:c.234+289G>A	ENSP00000436695.3:n.234+289G>A
ENST00000530704.6:c.298G>A	ENSP00000431655.1:p.Ala100Thr
ENST00000641083.1:c.276G>A
ENST00000641236.1:n.535G>A
ENST00000641319.1:c.298G>A	ENSP00000493128.1:p.Ala100Thr
ENST00000641471.1:c.385G>A	ENSP00000493146.1:p.Ala129Thr
ENST00000641548.1:c.*150G>A	ENSP00000492984.1:n.*150G>A
ENST00000641691.1:c.*150G>A	ENSP00000492910.1:n.*150G>A
ENST00000641924.1:c.124+5006G>A	ENSP00000493063.1:n.124+5006G>A
ENST00000642050.2:c.298G>A MANE Select	ENSP00000493153.1:p.Ala100Thr
ENST00000372779.8:c.385G>A	ENSP00000361865.4:p.Ala129Thr
ENST00000433473.7:c.298G>A	ENSP00000394863.3:p.Ala100Thr
ENST00000449045.6:c.125-2597G>A	ENSP00000392293.2:n.125-2597G>A
ENST00000526547.1:c.148G>A	ENSP00000436481.1:p.Ala50Thr
ENST00000527311.6:c.125-52G>A	ENSP00000436695.2:n.125-52G>A
ENST00000529905.5:c.298G>A	ENSP00000432053.1:p.Ala100Thr
ENST00000530704.5:c.298G>A	ENSP00000431655.1:p.Ala100Thr
NM_000310.3:c.298G>A , LRG_690t1:c.298G>A	NP_000301.1:p.Ala100Thr
NM_001142604.1:c.125-2597G>A	NP_001136076.1:n.125-2597G>A
XM_005271008.1:c.298G>A	XP_005271065.1:p.Ala100Thr
NM_001363695.1:c.298G>A	NP_001350624.1:p.Ala100Thr
NM_000310.4:c.298G>A MANE Select	NP_000301.1:p.Ala100Thr
NM_001142604.2:c.125-2597G>A	NP_001136076.1:n.125-2597G>A
NM_001363695.2:c.298G>A	NP_001350624.1:p.Ala100Thr