Canonical Allele Identifier: CA339845545

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40539791T>A (hg19) ; chr1:g.40074119T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074119T>A , CM000663.2:g.40074119T>A	GRCh38
NC_000001.10:g.40539791T>A , CM000663.1:g.40539791T>A	GRCh37
NC_000001.9:g.40312378T>A	NCBI36
NG_009192.1:g.28352A>T , LRG_690:g.28352A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.860A>T	ENSP00000394863.4:p.Asp287Val
ENST00000439754.6:c.791A>T	ENSP00000403207.2:p.Asp264Val
ENST00000449045.7:c.554A>T	ENSP00000392293.2:p.Asp185Val
ENST00000530076.6:c.206A>T	ENSP00000434007.1:p.Asp69Val
ENST00000530704.6:c.*486A>T	ENSP00000431655.1:n.*486A>T
ENST00000641083.1:c.953A>T
ENST00000641236.1:n.1100A>T
ENST00000641319.1:c.*73A>T	ENSP00000493128.1:n.*73A>T
ENST00000641381.1:c.285A>T
ENST00000641471.1:c.950A>T	ENSP00000493146.1:p.Asp317Val
ENST00000641691.1:c.*715A>T	ENSP00000492910.1:n.*715A>T
ENST00000641924.1:c.*292A>T	ENSP00000493063.1:n.*292A>T
ENST00000642050.2:c.863A>T MANE Select	ENSP00000493153.1:p.Asp288Val
ENST00000372775.2:n.260A>T
ENST00000433473.7:c.863A>T	ENSP00000394863.3:p.Asp288Val
ENST00000439754.5:c.476A>T	ENSP00000403207.1:p.Asp159Val
ENST00000449045.6:c.554A>T	ENSP00000392293.2:p.Asp185Val
ENST00000529905.5:c.863A>T	ENSP00000432053.1:p.Asp288Val
ENST00000530076.5:c.206A>T	ENSP00000434007.1:p.Asp69Val
ENST00000530704.5:c.*486A>T	ENSP00000431655.1:n.*486A>T
NM_000310.3:c.863A>T , LRG_690t1:c.863A>T	NP_000301.1:p.Asp288Val
NM_001142604.1:c.554A>T	NP_001136076.1:p.Asp185Val
XM_005271008.1:c.791A>T	XP_005271065.1:p.Asp264Val
NM_001363695.1:c.791A>T	NP_001350624.1:p.Asp264Val
NM_000310.4:c.863A>T MANE Select	NP_000301.1:p.Asp288Val
NM_001142604.2:c.554A>T	NP_001136076.1:p.Asp185Val
NM_001363695.2:c.791A>T	NP_001350624.1:p.Asp264Val