Canonical Allele Identifier: CA1164252056
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40092019_40092021delinsGTA , CM000663.2:g.40092019_40092021delinsGTA GRCh38
NC_000001.10:g.40557691_40557693delinsGTA , CM000663.1:g.40557691_40557693delinsGTA GRCh37
NC_000001.9:g.40330278_40330280delinsGTA NCBI36
NG_009192.1:g.10450_10452delinsTAC , LRG_690:g.10450_10452delinsTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.*198+24_*198+26delinsTAC ENSP00000361865.5:n.*198+24_*198+26delins...
ENST00000433473.8:c.359+24_359+26delinsTAC ENSP00000394863.4:n.359+24_359+26delinsTA...
ENST00000439754.6:c.362+24_362+26delinsTAC ENSP00000403207.2:n.362+24_362+26delinsTA...
ENST00000449045.7:c.125-2509_125-2507delinsTAC ENSP00000392293.2:n.125-2509_125-2507deli...
ENST00000526547.2:c.642+24_642+26delinsTAC
ENST00000527311.7:c.234+377_234+379delinsTAC ENSP00000436695.3:n.234+377_234+379delins...
ENST00000530704.6:c.362+24_362+26delinsTAC ENSP00000431655.1:n.362+24_362+26delinsTA...
ENST00000641083.1:c.340+24_340+26delinsTAC
ENST00000641236.1:n.599+24_599+26delinsTAC
ENST00000641319.1:c.362+24_362+26delinsTAC ENSP00000493128.1:n.362+24_362+26delinsTA...
ENST00000641471.1:c.449+24_449+26delinsTAC ENSP00000493146.1:n.449+24_449+26delinsTA...
ENST00000641548.1:c.*214+24_*214+26delinsTAC ENSP00000492984.1:n.*214+24_*214+26delins...
ENST00000641691.1:c.*214+24_*214+26delinsTAC ENSP00000492910.1:n.*214+24_*214+26delins...
ENST00000641924.1:c.124+5094_124+5096delinsTAC ENSP00000493063.1:n.124+5094_124+5096deli...
ENST00000642050.2:c.362+24_362+26delinsTAC MANE Select ENSP00000493153.1:n.362+24_362+26delinsTA...
ENST00000372779.8:c.449+24_449+26delinsTAC ENSP00000361865.4:n.449+24_449+26delinsTA...
ENST00000433473.7:c.362+24_362+26delinsTAC ENSP00000394863.3:n.362+24_362+26delinsTA...
ENST00000439754.5:c.47+24_47+26delinsTAC ENSP00000403207.1:n.47+24_47+26delinsTAC
ENST00000449045.6:c.125-2509_125-2507delinsTAC ENSP00000392293.2:n.125-2509_125-2507deli...
ENST00000526547.1:c.212+24_212+26delinsTAC ENSP00000436481.1:n.212+24_212+26delinsTA...
ENST00000527311.6:c.137+24_137+26delinsTAC ENSP00000436695.2:n.137+24_137+26delinsTA...
ENST00000529905.5:c.362+24_362+26delinsTAC ENSP00000432053.1:n.362+24_362+26delinsTA...
ENST00000530704.5:c.362+24_362+26delinsTAC ENSP00000431655.1:n.362+24_362+26delinsTA...
NM_000310.3:c.362+24_362+26delinsTAC , LRG_690t1:c.362+24_362+26delinsTAC NP_000301.1:n.362+24_362+26delinsTAC
NM_001142604.1:c.125-2509_125-2507delinsTAC NP_001136076.1:n.125-2509_125-2507delinsT...
XM_005271008.1:c.362+24_362+26delinsTAC XP_005271065.1:n.362+24_362+26delinsTAC
NM_001363695.1:c.362+24_362+26delinsTAC NP_001350624.1:n.362+24_362+26delinsTAC
NM_000310.4:c.362+24_362+26delinsTAC MANE Select NP_000301.1:n.362+24_362+26delinsTAC
NM_001142604.2:c.125-2509_125-2507delinsTAC NP_001136076.1:n.125-2509_125-2507delinsT...
NM_001363695.2:c.362+24_362+26delinsTAC NP_001350624.1:n.362+24_362+26delinsTAC