Canonical Allele Identifier: CA1164245680
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078901_40078904delinsTATA , CM000663.2:g.40078901_40078904delinsTATA GRCh38
NC_000001.10:g.40544573_40544576delinsTATA , CM000663.1:g.40544573_40544576delinsTATA GRCh37
NC_000001.9:g.40317160_40317163delinsTATA NCBI36
NG_009192.1:g.23567_23570delinsTATA , LRG_690:g.23567_23570delinsTATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.625-246_625-243delinsTATA ENSP00000394863.4:n.625-246_625-243delinsTATA
ENST00000439754.6:c.628-246_628-243delinsTATA ENSP00000403207.2:n.628-246_628-243delinsTATA
ENST00000449045.7:c.319-246_319-243delinsTATA ENSP00000392293.2:n.319-246_319-243delinsTATA
ENST00000527311.7:c.397-246_397-243delinsTATA ENSP00000436695.3:n.397-246_397-243delinsTATA
ENST00000530076.6:c.-30-246_-30-243delinsTATA ENSP00000434007.1:n.-30-246_-30-243delinsTATA
ENST00000530704.6:c.*251-246_*251-243delinsTATA ENSP00000431655.1:n.*251-246_*251-243delinsTATA
ENST00000641083.1:c.606-246_606-243delinsTATA
ENST00000641236.1:n.865-246_865-243delinsTATA
ENST00000641319.1:c.628-246_628-243delinsTATA ENSP00000493128.1:n.628-246_628-243delinsTATA
ENST00000641381.1:c.149-1991_149-1988delinsTATA
ENST00000641471.1:c.715-246_715-243delinsTATA ENSP00000493146.1:n.715-246_715-243delinsTATA
ENST00000641691.1:c.*480-246_*480-243delinsTATA ENSP00000492910.1:n.*480-246_*480-243delinsTATA
ENST00000641924.1:c.*57-246_*57-243delinsTATA ENSP00000493063.1:n.*57-246_*57-243delinsTATA
ENST00000642050.2:c.628-246_628-243delinsTATA MANE Select ENSP00000493153.1:n.628-246_628-243delinsTATA
ENST00000372779.8:c.715-246_715-243delinsTATA ENSP00000361865.4:n.715-246_715-243delinsTATA
ENST00000433473.7:c.628-246_628-243delinsTATA ENSP00000394863.3:n.628-246_628-243delinsTATA
ENST00000439754.5:c.313-246_313-243delinsTATA ENSP00000403207.1:n.313-246_313-243delinsTATA
ENST00000449045.6:c.319-246_319-243delinsTATA ENSP00000392293.2:n.319-246_319-243delinsTATA
ENST00000527311.6:c.403-246_403-243delinsTATA ENSP00000436695.2:n.403-246_403-243delinsTATA
ENST00000529905.5:c.628-246_628-243delinsTATA ENSP00000432053.1:n.628-246_628-243delinsTATA
ENST00000530076.5:c.-30-246_-30-243delinsTATA ENSP00000434007.1:n.-30-246_-30-243delinsTATA
ENST00000530704.5:c.*251-246_*251-243delinsTATA ENSP00000431655.1:n.*251-246_*251-243delinsTATA
NM_000310.3:c.628-246_628-243delinsTATA , LRG_690t1:c.628-246_628-243delinsTATA NP_000301.1:n.628-246_628-243delinsTATA
NM_001142604.1:c.319-246_319-243delinsTATA NP_001136076.1:n.319-246_319-243delinsTATA
XM_005271008.1:c.628-246_628-243delinsTATA XP_005271065.1:n.628-246_628-243delinsTATA
NM_001363695.1:c.628-246_628-243delinsTATA NP_001350624.1:n.628-246_628-243delinsTATA
NM_000310.4:c.628-246_628-243delinsTATA MANE Select NP_000301.1:n.628-246_628-243delinsTATA
NM_001142604.2:c.319-246_319-243delinsTATA NP_001136076.1:n.319-246_319-243delinsTATA
NM_001363695.2:c.628-246_628-243delinsTATA NP_001350624.1:n.628-246_628-243delinsTATA