Canonical Allele Identifier: CA2743276849

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091533_40091534insAGA , CM000663.2:g.40091533_40091534insAGA	GRCh38
NC_000001.10:g.40557205_40557206insAGA , CM000663.1:g.40557205_40557206insAGA	GRCh37
NC_000001.9:g.40329792_40329793insAGA	NCBI36
NG_009192.1:g.10937_10938insTCT , LRG_690:g.10937_10938insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*199-135_*199-134insTCT	ENSP00000361865.5:n.*199-135_*199-134insTCT
ENST00000433473.8:c.360-135_360-134insTCT	ENSP00000394863.4:n.360-135_360-134insTCT
ENST00000439754.6:c.363-135_363-134insTCT	ENSP00000403207.2:n.363-135_363-134insTCT
ENST00000449045.7:c.125-2022_125-2021insTCT	ENSP00000392293.2:n.125-2022_125-2021insTCT
ENST00000526547.2:c.643-135_643-134insTCT
ENST00000527311.7:c.235-135_235-134insTCT	ENSP00000436695.3:n.235-135_235-134insTCT
ENST00000530704.6:c.363-135_363-134insTCT	ENSP00000431655.1:n.363-135_363-134insTCT
ENST00000641083.1:c.341-135_341-134insTCT
ENST00000641236.1:n.600-135_600-134insTCT
ENST00000641319.1:c.363-135_363-134insTCT	ENSP00000493128.1:n.363-135_363-134insTCT
ENST00000641471.1:c.450-135_450-134insTCT	ENSP00000493146.1:n.450-135_450-134insTCT
ENST00000641548.1:c.*215-135_*215-134insTCT	ENSP00000492984.1:n.*215-135_*215-134insTCT
ENST00000641691.1:c.*215-135_*215-134insTCT	ENSP00000492910.1:n.*215-135_*215-134insTCT
ENST00000641924.1:c.124+5581_124+5582insTCT	ENSP00000493063.1:n.124+5581_124+5582insTCT
ENST00000642050.2:c.363-135_363-134insTCT MANE Select	ENSP00000493153.1:n.363-135_363-134insTCT
ENST00000372779.8:c.450-135_450-134insTCT	ENSP00000361865.4:n.450-135_450-134insTCT
ENST00000433473.7:c.363-135_363-134insTCT	ENSP00000394863.3:n.363-135_363-134insTCT
ENST00000439754.5:c.48-135_48-134insTCT	ENSP00000403207.1:n.48-135_48-134insTCT
ENST00000449045.6:c.125-2022_125-2021insTCT	ENSP00000392293.2:n.125-2022_125-2021insTCT
ENST00000526547.1:c.213-135_213-134insTCT	ENSP00000436481.1:n.213-135_213-134insTCT
ENST00000527311.6:c.138-135_138-134insTCT	ENSP00000436695.2:n.138-135_138-134insTCT
ENST00000529905.5:c.363-135_363-134insTCT	ENSP00000432053.1:n.363-135_363-134insTCT
ENST00000530704.5:c.363-135_363-134insTCT	ENSP00000431655.1:n.363-135_363-134insTCT
NM_000310.3:c.363-135_363-134insTCT , LRG_690t1:c.363-135_363-134insTCT	NP_000301.1:n.363-135_363-134insTCT
NM_001142604.1:c.125-2022_125-2021insTCT	NP_001136076.1:n.125-2022_125-2021insTCT
XM_005271008.1:c.363-135_363-134insTCT	XP_005271065.1:n.363-135_363-134insTCT
NM_001363695.1:c.363-135_363-134insTCT	NP_001350624.1:n.363-135_363-134insTCT
NM_000310.4:c.363-135_363-134insTCT MANE Select	NP_000301.1:n.363-135_363-134insTCT
NM_001142604.2:c.125-2022_125-2021insTCT	NP_001136076.1:n.125-2022_125-2021insTCT
NM_001363695.2:c.363-135_363-134insTCT	NP_001350624.1:n.363-135_363-134insTCT