Canonical Allele Identifier: CA2645092433

Gene: PPT1

Linked Data

• gnomAD v4: 1-40091513-T-TGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091513_40091514insGGG , CM000663.2:g.40091513_40091514insGGG	GRCh38
NC_000001.10:g.40557185_40557186insGGG , CM000663.1:g.40557185_40557186insGGG	GRCh37
NC_000001.9:g.40329772_40329773insGGG	NCBI36
NG_009192.1:g.10957_10958insCCC , LRG_690:g.10957_10958insCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*199-115_*199-114insCCC	ENSP00000361865.5:n.*199-115_*199-114insCCC
ENST00000433473.8:c.360-115_360-114insCCC	ENSP00000394863.4:n.360-115_360-114insCCC
ENST00000439754.6:c.363-115_363-114insCCC	ENSP00000403207.2:n.363-115_363-114insCCC
ENST00000449045.7:c.125-2002_125-2001insCCC	ENSP00000392293.2:n.125-2002_125-2001insCCC
ENST00000526547.2:c.643-115_643-114insCCC
ENST00000527311.7:c.235-115_235-114insCCC	ENSP00000436695.3:n.235-115_235-114insCCC
ENST00000530704.6:c.363-115_363-114insCCC	ENSP00000431655.1:n.363-115_363-114insCCC
ENST00000641083.1:c.341-115_341-114insCCC
ENST00000641236.1:n.600-115_600-114insCCC
ENST00000641319.1:c.363-115_363-114insCCC	ENSP00000493128.1:n.363-115_363-114insCCC
ENST00000641471.1:c.450-115_450-114insCCC	ENSP00000493146.1:n.450-115_450-114insCCC
ENST00000641548.1:c.*215-115_*215-114insCCC	ENSP00000492984.1:n.*215-115_*215-114insCCC
ENST00000641691.1:c.*215-115_*215-114insCCC	ENSP00000492910.1:n.*215-115_*215-114insCCC
ENST00000641924.1:c.124+5601_124+5602insCCC	ENSP00000493063.1:n.124+5601_124+5602insCCC
ENST00000642050.2:c.363-115_363-114insCCC MANE Select	ENSP00000493153.1:n.363-115_363-114insCCC
ENST00000372779.8:c.450-115_450-114insCCC	ENSP00000361865.4:n.450-115_450-114insCCC
ENST00000433473.7:c.363-115_363-114insCCC	ENSP00000394863.3:n.363-115_363-114insCCC
ENST00000439754.5:c.48-115_48-114insCCC	ENSP00000403207.1:n.48-115_48-114insCCC
ENST00000449045.6:c.125-2002_125-2001insCCC	ENSP00000392293.2:n.125-2002_125-2001insCCC
ENST00000526547.1:c.213-115_213-114insCCC	ENSP00000436481.1:n.213-115_213-114insCCC
ENST00000527311.6:c.138-115_138-114insCCC	ENSP00000436695.2:n.138-115_138-114insCCC
ENST00000529905.5:c.363-115_363-114insCCC	ENSP00000432053.1:n.363-115_363-114insCCC
ENST00000530704.5:c.363-115_363-114insCCC	ENSP00000431655.1:n.363-115_363-114insCCC
NM_000310.3:c.363-115_363-114insCCC , LRG_690t1:c.363-115_363-114insCCC	NP_000301.1:n.363-115_363-114insCCC
NM_001142604.1:c.125-2002_125-2001insCCC	NP_001136076.1:n.125-2002_125-2001insCCC
XM_005271008.1:c.363-115_363-114insCCC	XP_005271065.1:n.363-115_363-114insCCC
NM_001363695.1:c.363-115_363-114insCCC	NP_001350624.1:n.363-115_363-114insCCC
NM_000310.4:c.363-115_363-114insCCC MANE Select	NP_000301.1:n.363-115_363-114insCCC
NM_001142604.2:c.125-2002_125-2001insCCC	NP_001136076.1:n.125-2002_125-2001insCCC
NM_001363695.2:c.363-115_363-114insCCC	NP_001350624.1:n.363-115_363-114insCCC