Canonical Allele Identifier: CA2743276753

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091497_40091498insAGT , CM000663.2:g.40091497_40091498insAGT	GRCh38
NC_000001.10:g.40557169_40557170insAGT , CM000663.1:g.40557169_40557170insAGT	GRCh37
NC_000001.9:g.40329756_40329757insAGT	NCBI36
NG_009192.1:g.10973_10974insACT , LRG_690:g.10973_10974insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*199-99_*199-98insACT	ENSP00000361865.5:n.*199-99_*199-98insACT
ENST00000433473.8:c.360-99_360-98insACT	ENSP00000394863.4:n.360-99_360-98insACT
ENST00000439754.6:c.363-99_363-98insACT	ENSP00000403207.2:n.363-99_363-98insACT
ENST00000449045.7:c.125-1986_125-1985insACT	ENSP00000392293.2:n.125-1986_125-1985insACT
ENST00000526547.2:c.643-99_643-98insACT
ENST00000527311.7:c.235-99_235-98insACT	ENSP00000436695.3:n.235-99_235-98insACT
ENST00000530704.6:c.363-99_363-98insACT	ENSP00000431655.1:n.363-99_363-98insACT
ENST00000641083.1:c.341-99_341-98insACT
ENST00000641236.1:n.600-99_600-98insACT
ENST00000641319.1:c.363-99_363-98insACT	ENSP00000493128.1:n.363-99_363-98insACT
ENST00000641471.1:c.450-99_450-98insACT	ENSP00000493146.1:n.450-99_450-98insACT
ENST00000641548.1:c.*215-99_*215-98insACT	ENSP00000492984.1:n.*215-99_*215-98insACT
ENST00000641691.1:c.*215-99_*215-98insACT	ENSP00000492910.1:n.*215-99_*215-98insACT
ENST00000641924.1:c.124+5617_124+5618insACT	ENSP00000493063.1:n.124+5617_124+5618insACT
ENST00000642050.2:c.363-99_363-98insACT MANE Select	ENSP00000493153.1:n.363-99_363-98insACT
ENST00000372779.8:c.450-99_450-98insACT	ENSP00000361865.4:n.450-99_450-98insACT
ENST00000433473.7:c.363-99_363-98insACT	ENSP00000394863.3:n.363-99_363-98insACT
ENST00000439754.5:c.48-99_48-98insACT	ENSP00000403207.1:n.48-99_48-98insACT
ENST00000449045.6:c.125-1986_125-1985insACT	ENSP00000392293.2:n.125-1986_125-1985insACT
ENST00000526547.1:c.213-99_213-98insACT	ENSP00000436481.1:n.213-99_213-98insACT
ENST00000527311.6:c.138-99_138-98insACT	ENSP00000436695.2:n.138-99_138-98insACT
ENST00000529905.5:c.363-99_363-98insACT	ENSP00000432053.1:n.363-99_363-98insACT
ENST00000530704.5:c.363-99_363-98insACT	ENSP00000431655.1:n.363-99_363-98insACT
NM_000310.3:c.363-99_363-98insACT , LRG_690t1:c.363-99_363-98insACT	NP_000301.1:n.363-99_363-98insACT
NM_001142604.1:c.125-1986_125-1985insACT	NP_001136076.1:n.125-1986_125-1985insACT
XM_005271008.1:c.363-99_363-98insACT	XP_005271065.1:n.363-99_363-98insACT
NM_001363695.1:c.363-99_363-98insACT	NP_001350624.1:n.363-99_363-98insACT
NM_000310.4:c.363-99_363-98insACT MANE Select	NP_000301.1:n.363-99_363-98insACT
NM_001142604.2:c.125-1986_125-1985insACT	NP_001136076.1:n.125-1986_125-1985insACT
NM_001363695.2:c.363-99_363-98insACT	NP_001350624.1:n.363-99_363-98insACT