Canonical Allele Identifier: CA339848796

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557001C>A (hg19) ; chr1:g.40091329C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091329C>A , CM000663.2:g.40091329C>A	GRCh38
NC_000001.10:g.40557001C>A , CM000663.1:g.40557001C>A	GRCh37
NC_000001.9:g.40329588C>A	NCBI36
NG_009192.1:g.11142G>T , LRG_690:g.11142G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000372779.9:c.*269G>T	ENSP00000361865.5:n.*269G>T
ENST00000433473.8:c.430G>T	ENSP00000394863.4:p.Gly144Cys
ENST00000439754.6:c.433G>T	ENSP00000403207.2:p.Gly145Cys
ENST00000449045.7:c.125-1817G>T	ENSP00000392293.2:n.125-1817G>T
ENST00000526547.2:c.713G>T
ENST00000527311.7:c.305G>T	ENSP00000436695.3:p.Ser102Ile
ENST00000530704.6:c.433G>T	ENSP00000431655.1:p.Val145Leu
ENST00000641083.1:c.411G>T
ENST00000641236.1:n.670G>T
ENST00000641319.1:c.433G>T	ENSP00000493128.1:p.Gly145Cys
ENST00000641381.1:c.45G>T
ENST00000641471.1:c.520G>T	ENSP00000493146.1:p.Gly174Cys
ENST00000641548.1:c.*285G>T	ENSP00000492984.1:n.*285G>T
ENST00000641691.1:c.*285G>T	ENSP00000492910.1:n.*285G>T
ENST00000641924.1:c.124+5786G>T	ENSP00000493063.1:n.124+5786G>T
ENST00000642050.2:c.433G>T MANE Select	ENSP00000493153.1:p.Gly145Cys
ENST00000372779.8:c.520G>T	ENSP00000361865.4:p.Gly174Cys
ENST00000433473.7:c.433G>T	ENSP00000394863.3:p.Gly145Cys
ENST00000439754.5:c.118G>T	ENSP00000403207.1:p.Gly40Cys
ENST00000449045.6:c.125-1817G>T	ENSP00000392293.2:n.125-1817G>T
ENST00000526547.1:c.283G>T	ENSP00000436481.1:p.Gly95Cys
ENST00000527311.6:c.208G>T	ENSP00000436695.2:p.Gly70Cys
ENST00000529905.5:c.433G>T	ENSP00000432053.1:p.Gly145Cys
ENST00000530704.5:c.433G>T	ENSP00000431655.1:p.Val145Leu
NM_000310.3:c.433G>T , LRG_690t1:c.433G>T	NP_000301.1:p.Gly145Cys
NM_001142604.1:c.125-1817G>T	NP_001136076.1:n.125-1817G>T
XM_005271008.1:c.433G>T	XP_005271065.1:p.Gly145Cys
NM_001363695.1:c.433G>T	NP_001350624.1:p.Gly145Cys
NM_000310.4:c.433G>T MANE Select	NP_000301.1:p.Gly145Cys
NM_001142604.2:c.125-1817G>T	NP_001136076.1:n.125-1817G>T
NM_001363695.2:c.433G>T	NP_001350624.1:p.Gly145Cys