Canonical Allele Identifier: CA2743276788
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40091506_40091508del , CM000663.2:g.40091506_40091508del GRCh38
NC_000001.10:g.40557178_40557180del , CM000663.1:g.40557178_40557180del GRCh37
NC_000001.9:g.40329765_40329767del NCBI36
NG_009192.1:g.10964_10966del , LRG_690:g.10964_10966del

Transcript Alleles

HGVS Amino-acid Change
ENST00000372779.9:c.*199-108_*199-106del ENSP00000361865.5:n.*199-108_*199-106del
ENST00000433473.8:c.360-108_360-106del ENSP00000394863.4:n.360-108_360-106del
ENST00000439754.6:c.363-108_363-106del ENSP00000403207.2:n.363-108_363-106del
ENST00000449045.7:c.125-1995_125-1993del ENSP00000392293.2:n.125-1995_125-1993del
ENST00000526547.2:c.643-108_643-106del
ENST00000527311.7:c.235-108_235-106del ENSP00000436695.3:n.235-108_235-106del
ENST00000530704.6:c.363-108_363-106del ENSP00000431655.1:n.363-108_363-106del
ENST00000641083.1:c.341-108_341-106del
ENST00000641236.1:n.600-108_600-106del
ENST00000641319.1:c.363-108_363-106del ENSP00000493128.1:n.363-108_363-106del
ENST00000641471.1:c.450-108_450-106del ENSP00000493146.1:n.450-108_450-106del
ENST00000641548.1:c.*215-108_*215-106del ENSP00000492984.1:n.*215-108_*215-106del
ENST00000641691.1:c.*215-108_*215-106del ENSP00000492910.1:n.*215-108_*215-106del
ENST00000641924.1:c.124+5608_124+5610del ENSP00000493063.1:n.124+5608_124+5610del
ENST00000642050.2:c.363-108_363-106del MANE Select ENSP00000493153.1:n.363-108_363-106del
ENST00000372779.8:c.450-108_450-106del ENSP00000361865.4:n.450-108_450-106del
ENST00000433473.7:c.363-108_363-106del ENSP00000394863.3:n.363-108_363-106del
ENST00000439754.5:c.48-108_48-106del ENSP00000403207.1:n.48-108_48-106del
ENST00000449045.6:c.125-1995_125-1993del ENSP00000392293.2:n.125-1995_125-1993del
ENST00000526547.1:c.213-108_213-106del ENSP00000436481.1:n.213-108_213-106del
ENST00000527311.6:c.138-108_138-106del ENSP00000436695.2:n.138-108_138-106del
ENST00000529905.5:c.363-108_363-106del ENSP00000432053.1:n.363-108_363-106del
ENST00000530704.5:c.363-108_363-106del ENSP00000431655.1:n.363-108_363-106del
NM_000310.3:c.363-108_363-106del , LRG_690t1:c.363-108_363-106del NP_000301.1:n.363-108_363-106del
NM_001142604.1:c.125-1995_125-1993del NP_001136076.1:n.125-1995_125-1993del
XM_005271008.1:c.363-108_363-106del XP_005271065.1:n.363-108_363-106del
NM_001363695.1:c.363-108_363-106del NP_001350624.1:n.363-108_363-106del
NM_000310.4:c.363-108_363-106del MANE Select NP_000301.1:n.363-108_363-106del
NM_001142604.2:c.125-1995_125-1993del NP_001136076.1:n.125-1995_125-1993del
NM_001363695.2:c.363-108_363-106del NP_001350624.1:n.363-108_363-106del