Canonical Allele Identifier: CA339846655

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40544258A>T (hg19) ; chr1:g.40078586A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40078586A>T , CM000663.2:g.40078586A>T	GRCh38
NC_000001.10:g.40544258A>T , CM000663.1:g.40544258A>T	GRCh37
NC_000001.9:g.40316845A>T	NCBI36
NG_009192.1:g.23885T>A , LRG_690:g.23885T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.697T>A	ENSP00000394863.4:p.Ser233Thr
ENST00000439754.6:c.700T>A	ENSP00000403207.2:p.Ser234Thr
ENST00000449045.7:c.391T>A	ENSP00000392293.2:p.Ser131Thr
ENST00000527311.7:c.469T>A	ENSP00000436695.3:p.Ser157Thr
ENST00000530076.6:c.43T>A	ENSP00000434007.1:p.Ser15Thr
ENST00000530704.6:c.*323T>A	ENSP00000431655.1:n.*323T>A
ENST00000641083.1:c.678T>A
ENST00000641236.1:n.937T>A
ENST00000641319.1:c.700T>A	ENSP00000493128.1:p.Ser234Thr
ENST00000641381.1:c.149-1673T>A
ENST00000641471.1:c.787T>A	ENSP00000493146.1:p.Ser263Thr
ENST00000641691.1:c.*552T>A	ENSP00000492910.1:n.*552T>A
ENST00000641924.1:c.*129T>A	ENSP00000493063.1:n.*129T>A
ENST00000642050.2:c.700T>A MANE Select	ENSP00000493153.1:p.Ser234Thr
ENST00000372775.2:n.97T>A
ENST00000372779.8:c.787T>A	ENSP00000361865.4:p.Ser263Thr
ENST00000433473.7:c.700T>A	ENSP00000394863.3:p.Ser234Thr
ENST00000439754.5:c.385T>A	ENSP00000403207.1:p.Ser129Thr
ENST00000449045.6:c.391T>A	ENSP00000392293.2:p.Ser131Thr
ENST00000527311.6:c.475T>A	ENSP00000436695.2:p.Ser159Thr
ENST00000529905.5:c.700T>A	ENSP00000432053.1:p.Ser234Thr
ENST00000530076.5:c.43T>A	ENSP00000434007.1:p.Ser15Thr
ENST00000530704.5:c.*323T>A	ENSP00000431655.1:n.*323T>A
NM_000310.3:c.700T>A , LRG_690t1:c.700T>A	NP_000301.1:p.Ser234Thr
NM_001142604.1:c.391T>A	NP_001136076.1:p.Ser131Thr
XM_005271008.1:c.700T>A	XP_005271065.1:p.Ser234Thr
NM_001363695.1:c.700T>A	NP_001350624.1:p.Ser234Thr
NM_000310.4:c.700T>A MANE Select	NP_000301.1:p.Ser234Thr
NM_001142604.2:c.391T>A	NP_001136076.1:p.Ser131Thr
NM_001363695.2:c.700T>A	NP_001350624.1:p.Ser234Thr