Canonical Allele Identifier: CA1141587661
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078899_40078903delinsGGTAT , CM000663.2:g.40078899_40078903delinsGGTAT GRCh38
NC_000001.10:g.40544571_40544575delinsGGTAT , CM000663.1:g.40544571_40544575delinsGGTAT GRCh37
NC_000001.9:g.40317158_40317162delinsGGTAT NCBI36
NG_009192.1:g.23568_23572delinsATACC , LRG_690:g.23568_23572delinsATACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.625-245_625-241delinsATACC ENSP00000394863.4:n.625-245_625-241delinsATACC
ENST00000439754.6:c.628-245_628-241delinsATACC ENSP00000403207.2:n.628-245_628-241delinsATACC
ENST00000449045.7:c.319-245_319-241delinsATACC ENSP00000392293.2:n.319-245_319-241delinsATACC
ENST00000527311.7:c.397-245_397-241delinsATACC ENSP00000436695.3:n.397-245_397-241delinsATACC
ENST00000530076.6:c.-30-245_-30-241delinsATACC ENSP00000434007.1:n.-30-245_-30-241delinsATACC
ENST00000530704.6:c.*251-245_*251-241delinsATACC ENSP00000431655.1:n.*251-245_*251-241delinsATACC
ENST00000641083.1:c.606-245_606-241delinsATACC
ENST00000641236.1:n.865-245_865-241delinsATACC
ENST00000641319.1:c.628-245_628-241delinsATACC ENSP00000493128.1:n.628-245_628-241delinsATACC
ENST00000641381.1:c.149-1990_149-1986delinsATACC
ENST00000641471.1:c.715-245_715-241delinsATACC ENSP00000493146.1:n.715-245_715-241delinsATACC
ENST00000641691.1:c.*480-245_*480-241delinsATACC ENSP00000492910.1:n.*480-245_*480-241delinsATACC
ENST00000641924.1:c.*57-245_*57-241delinsATACC ENSP00000493063.1:n.*57-245_*57-241delinsATACC
ENST00000642050.2:c.628-245_628-241delinsATACC MANE Select ENSP00000493153.1:n.628-245_628-241delinsATACC
ENST00000372779.8:c.715-245_715-241delinsATACC ENSP00000361865.4:n.715-245_715-241delinsATACC
ENST00000433473.7:c.628-245_628-241delinsATACC ENSP00000394863.3:n.628-245_628-241delinsATACC
ENST00000439754.5:c.313-245_313-241delinsATACC ENSP00000403207.1:n.313-245_313-241delinsATACC
ENST00000449045.6:c.319-245_319-241delinsATACC ENSP00000392293.2:n.319-245_319-241delinsATACC
ENST00000527311.6:c.403-245_403-241delinsATACC ENSP00000436695.2:n.403-245_403-241delinsATACC
ENST00000529905.5:c.628-245_628-241delinsATACC ENSP00000432053.1:n.628-245_628-241delinsATACC
ENST00000530076.5:c.-30-245_-30-241delinsATACC ENSP00000434007.1:n.-30-245_-30-241delinsATACC
ENST00000530704.5:c.*251-245_*251-241delinsATACC ENSP00000431655.1:n.*251-245_*251-241delinsATACC
NM_000310.3:c.628-245_628-241delinsATACC , LRG_690t1:c.628-245_628-241delinsATACC NP_000301.1:n.628-245_628-241delinsATACC
NM_001142604.1:c.319-245_319-241delinsATACC NP_001136076.1:n.319-245_319-241delinsATACC
XM_005271008.1:c.628-245_628-241delinsATACC XP_005271065.1:n.628-245_628-241delinsATACC
NM_001363695.1:c.628-245_628-241delinsATACC NP_001350624.1:n.628-245_628-241delinsATACC
NM_000310.4:c.628-245_628-241delinsATACC MANE Select NP_000301.1:n.628-245_628-241delinsATACC
NM_001142604.2:c.319-245_319-241delinsATACC NP_001136076.1:n.319-245_319-241delinsATACC
NM_001363695.2:c.628-245_628-241delinsATACC NP_001350624.1:n.628-245_628-241delinsATACC