Canonical Allele Identifier: CA2743276939

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091569_40091570del , CM000663.2:g.40091569_40091570del	GRCh38
NC_000001.10:g.40557241_40557242del , CM000663.1:g.40557241_40557242del	GRCh37
NC_000001.9:g.40329828_40329829del	NCBI36
NG_009192.1:g.10902_10903del , LRG_690:g.10902_10903del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*199-170_*199-169del	ENSP00000361865.5:n.*199-170_*199-169del
ENST00000433473.8:c.360-170_360-169del	ENSP00000394863.4:n.360-170_360-169del
ENST00000439754.6:c.363-170_363-169del	ENSP00000403207.2:n.363-170_363-169del
ENST00000449045.7:c.125-2057_125-2056del	ENSP00000392293.2:n.125-2057_125-2056del
ENST00000526547.2:c.643-170_643-169del
ENST00000527311.7:c.235-170_235-169del	ENSP00000436695.3:n.235-170_235-169del
ENST00000530704.6:c.363-170_363-169del	ENSP00000431655.1:n.363-170_363-169del
ENST00000641083.1:c.341-170_341-169del
ENST00000641236.1:n.600-170_600-169del
ENST00000641319.1:c.363-170_363-169del	ENSP00000493128.1:n.363-170_363-169del
ENST00000641471.1:c.450-170_450-169del	ENSP00000493146.1:n.450-170_450-169del
ENST00000641548.1:c.*215-170_*215-169del	ENSP00000492984.1:n.*215-170_*215-169del
ENST00000641691.1:c.*215-170_*215-169del	ENSP00000492910.1:n.*215-170_*215-169del
ENST00000641924.1:c.124+5546_124+5547del	ENSP00000493063.1:n.124+5546_124+5547del
ENST00000642050.2:c.363-170_363-169del MANE Select	ENSP00000493153.1:n.363-170_363-169del
ENST00000372779.8:c.450-170_450-169del	ENSP00000361865.4:n.450-170_450-169del
ENST00000433473.7:c.363-170_363-169del	ENSP00000394863.3:n.363-170_363-169del
ENST00000439754.5:c.48-170_48-169del	ENSP00000403207.1:n.48-170_48-169del
ENST00000449045.6:c.125-2057_125-2056del	ENSP00000392293.2:n.125-2057_125-2056del
ENST00000526547.1:c.213-170_213-169del	ENSP00000436481.1:n.213-170_213-169del
ENST00000527311.6:c.138-170_138-169del	ENSP00000436695.2:n.138-170_138-169del
ENST00000529905.5:c.363-170_363-169del	ENSP00000432053.1:n.363-170_363-169del
ENST00000530704.5:c.363-170_363-169del	ENSP00000431655.1:n.363-170_363-169del
NM_000310.3:c.363-170_363-169del , LRG_690t1:c.363-170_363-169del	NP_000301.1:n.363-170_363-169del
NM_001142604.1:c.125-2057_125-2056del	NP_001136076.1:n.125-2057_125-2056del
XM_005271008.1:c.363-170_363-169del	XP_005271065.1:n.363-170_363-169del
NM_001363695.1:c.363-170_363-169del	NP_001350624.1:n.363-170_363-169del
NM_000310.4:c.363-170_363-169del MANE Select	NP_000301.1:n.363-170_363-169del
NM_001142604.2:c.125-2057_125-2056del	NP_001136076.1:n.125-2057_125-2056del
NM_001363695.2:c.363-170_363-169del	NP_001350624.1:n.363-170_363-169del