Canonical Allele Identifier: CA2743276839

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091529_40091530insC , CM000663.2:g.40091529_40091530insC	GRCh38
NC_000001.10:g.40557201_40557202insC , CM000663.1:g.40557201_40557202insC	GRCh37
NC_000001.9:g.40329788_40329789insC	NCBI36
NG_009192.1:g.10941_10942insG , LRG_690:g.10941_10942insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*199-131_*199-130insG	ENSP00000361865.5:n.*199-131_*199-130insG
ENST00000433473.8:c.360-131_360-130insG	ENSP00000394863.4:n.360-131_360-130insG
ENST00000439754.6:c.363-131_363-130insG	ENSP00000403207.2:n.363-131_363-130insG
ENST00000449045.7:c.125-2018_125-2017insG	ENSP00000392293.2:n.125-2018_125-2017insG
ENST00000526547.2:c.643-131_643-130insG
ENST00000527311.7:c.235-131_235-130insG	ENSP00000436695.3:n.235-131_235-130insG
ENST00000530704.6:c.363-131_363-130insG	ENSP00000431655.1:n.363-131_363-130insG
ENST00000641083.1:c.341-131_341-130insG
ENST00000641236.1:n.600-131_600-130insG
ENST00000641319.1:c.363-131_363-130insG	ENSP00000493128.1:n.363-131_363-130insG
ENST00000641471.1:c.450-131_450-130insG	ENSP00000493146.1:n.450-131_450-130insG
ENST00000641548.1:c.*215-131_*215-130insG	ENSP00000492984.1:n.*215-131_*215-130insG
ENST00000641691.1:c.*215-131_*215-130insG	ENSP00000492910.1:n.*215-131_*215-130insG
ENST00000641924.1:c.124+5585_124+5586insG	ENSP00000493063.1:n.124+5585_124+5586insG
ENST00000642050.2:c.363-131_363-130insG MANE Select	ENSP00000493153.1:n.363-131_363-130insG
ENST00000372779.8:c.450-131_450-130insG	ENSP00000361865.4:n.450-131_450-130insG
ENST00000433473.7:c.363-131_363-130insG	ENSP00000394863.3:n.363-131_363-130insG
ENST00000439754.5:c.48-131_48-130insG	ENSP00000403207.1:n.48-131_48-130insG
ENST00000449045.6:c.125-2018_125-2017insG	ENSP00000392293.2:n.125-2018_125-2017insG
ENST00000526547.1:c.213-131_213-130insG	ENSP00000436481.1:n.213-131_213-130insG
ENST00000527311.6:c.138-131_138-130insG	ENSP00000436695.2:n.138-131_138-130insG
ENST00000529905.5:c.363-131_363-130insG	ENSP00000432053.1:n.363-131_363-130insG
ENST00000530704.5:c.363-131_363-130insG	ENSP00000431655.1:n.363-131_363-130insG
NM_000310.3:c.363-131_363-130insG , LRG_690t1:c.363-131_363-130insG	NP_000301.1:n.363-131_363-130insG
NM_001142604.1:c.125-2018_125-2017insG	NP_001136076.1:n.125-2018_125-2017insG
XM_005271008.1:c.363-131_363-130insG	XP_005271065.1:n.363-131_363-130insG
NM_001363695.1:c.363-131_363-130insG	NP_001350624.1:n.363-131_363-130insG
NM_000310.4:c.363-131_363-130insG MANE Select	NP_000301.1:n.363-131_363-130insG
NM_001142604.2:c.125-2018_125-2017insG	NP_001136076.1:n.125-2018_125-2017insG
NM_001363695.2:c.363-131_363-130insG	NP_001350624.1:n.363-131_363-130insG