Canonical Allele Identifier: CA2743276846
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40091532_40091534del , CM000663.2:g.40091532_40091534del GRCh38
NC_000001.10:g.40557204_40557206del , CM000663.1:g.40557204_40557206del GRCh37
NC_000001.9:g.40329791_40329793del NCBI36
NG_009192.1:g.10937_10939del , LRG_690:g.10937_10939del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372779.9:c.*199-135_*199-133del ENSP00000361865.5:n.*199-135_*199-133del
ENST00000433473.8:c.360-135_360-133del ENSP00000394863.4:n.360-135_360-133del
ENST00000439754.6:c.363-135_363-133del ENSP00000403207.2:n.363-135_363-133del
ENST00000449045.7:c.125-2022_125-2020del ENSP00000392293.2:n.125-2022_125-2020del
ENST00000526547.2:c.643-135_643-133del
ENST00000527311.7:c.235-135_235-133del ENSP00000436695.3:n.235-135_235-133del
ENST00000530704.6:c.363-135_363-133del ENSP00000431655.1:n.363-135_363-133del
ENST00000641083.1:c.341-135_341-133del
ENST00000641236.1:n.600-135_600-133del
ENST00000641319.1:c.363-135_363-133del ENSP00000493128.1:n.363-135_363-133del
ENST00000641471.1:c.450-135_450-133del ENSP00000493146.1:n.450-135_450-133del
ENST00000641548.1:c.*215-135_*215-133del ENSP00000492984.1:n.*215-135_*215-133del
ENST00000641691.1:c.*215-135_*215-133del ENSP00000492910.1:n.*215-135_*215-133del
ENST00000641924.1:c.124+5581_124+5583del ENSP00000493063.1:n.124+5581_124+5583del
ENST00000642050.2:c.363-135_363-133del MANE Select ENSP00000493153.1:n.363-135_363-133del
ENST00000372779.8:c.450-135_450-133del ENSP00000361865.4:n.450-135_450-133del
ENST00000433473.7:c.363-135_363-133del ENSP00000394863.3:n.363-135_363-133del
ENST00000439754.5:c.48-135_48-133del ENSP00000403207.1:n.48-135_48-133del
ENST00000449045.6:c.125-2022_125-2020del ENSP00000392293.2:n.125-2022_125-2020del
ENST00000526547.1:c.213-135_213-133del ENSP00000436481.1:n.213-135_213-133del
ENST00000527311.6:c.138-135_138-133del ENSP00000436695.2:n.138-135_138-133del
ENST00000529905.5:c.363-135_363-133del ENSP00000432053.1:n.363-135_363-133del
ENST00000530704.5:c.363-135_363-133del ENSP00000431655.1:n.363-135_363-133del
NM_000310.3:c.363-135_363-133del , LRG_690t1:c.363-135_363-133del NP_000301.1:n.363-135_363-133del
NM_001142604.1:c.125-2022_125-2020del NP_001136076.1:n.125-2022_125-2020del
XM_005271008.1:c.363-135_363-133del XP_005271065.1:n.363-135_363-133del
NM_001363695.1:c.363-135_363-133del NP_001350624.1:n.363-135_363-133del
NM_000310.4:c.363-135_363-133del MANE Select NP_000301.1:n.363-135_363-133del
NM_001142604.2:c.125-2022_125-2020del NP_001136076.1:n.125-2022_125-2020del
NM_001363695.2:c.363-135_363-133del NP_001350624.1:n.363-135_363-133del