Canonical Allele Identifier: CA1164235651
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40080410A= , CM000663.2:g.40080410A= GRCh38
NC_000001.10:g.40546082A= , CM000663.1:g.40546082A= GRCh37
NC_000001.9:g.40318669A= NCBI36
NG_009192.1:g.22061T= , LRG_690:g.22061T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.611T= ENSP00000394863.4:p.Ile204=
ENST00000439754.6:c.614T= ENSP00000403207.2:p.Ile205=
ENST00000449045.7:c.305T= ENSP00000392293.2:p.Ile102=
ENST00000527311.7:c.383T= ENSP00000436695.3:p.Ile128=
ENST00000530076.6:c.-44T= ENSP00000434007.1:n.-44T=
ENST00000530704.6:c.*237T= ENSP00000431655.1:n.*237T=
ENST00000641083.1:c.592T=
ENST00000641236.1:n.851T=
ENST00000641319.1:c.614T= ENSP00000493128.1:p.Ile205=
ENST00000641381.1:c.149-3497T=
ENST00000641471.1:c.701T= ENSP00000493146.1:p.Ile234=
ENST00000641691.1:c.*466T= ENSP00000492910.1:n.*466T=
ENST00000641924.1:c.*43T= ENSP00000493063.1:n.*43T=
ENST00000642050.2:c.614T= MANE Select ENSP00000493153.1:p.Ile205=
ENST00000372779.8:c.701T= ENSP00000361865.4:p.Ile234=
ENST00000433473.7:c.614T= ENSP00000394863.3:p.Ile205=
ENST00000439754.5:c.299T= ENSP00000403207.1:p.Ile100=
ENST00000449045.6:c.305T= ENSP00000392293.2:p.Ile102=
ENST00000527311.6:c.389T= ENSP00000436695.2:p.Ile130=
ENST00000529905.5:c.614T= ENSP00000432053.1:p.Ile205=
ENST00000530076.5:c.-44T= ENSP00000434007.1:n.-44T=
ENST00000530704.5:c.*237T= ENSP00000431655.1:n.*237T=
NM_000310.3:c.614T= , LRG_690t1:c.614T= NP_000301.1:p.Ile205=
NM_001142604.1:c.305T= NP_001136076.1:p.Ile102=
XM_005271008.1:c.614T= XP_005271065.1:p.Ile205=
NM_001363695.1:c.614T= NP_001350624.1:p.Ile205=
NM_000310.4:c.614T= MANE Select NP_000301.1:p.Ile205=
NM_001142604.2:c.305T= NP_001136076.1:p.Ile102=
NM_001363695.2:c.614T= NP_001350624.1:p.Ile205=