Canonical Allele Identifier: CA1164252721
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40092442C= , CM000663.2:g.40092442C= GRCh38
NC_000001.10:g.40558114C= , CM000663.1:g.40558114C= GRCh37
NC_000001.9:g.40330701C= NCBI36
NG_009192.1:g.10029G= , LRG_690:g.10029G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372779.9:c.*26G= ENSP00000361865.5:n.*26G=
ENST00000433473.8:c.187G= ENSP00000394863.4:p.Gly63=
ENST00000439754.6:c.190G= ENSP00000403207.2:p.Gly64=
ENST00000449045.7:c.125-2930G= ENSP00000392293.2:n.125-2930G=
ENST00000526547.2:c.470G=
ENST00000527311.7:c.190G= ENSP00000436695.3:p.Gly64=
ENST00000530704.6:c.190G= ENSP00000431655.1:p.Gly64=
ENST00000641083.1:c.168G=
ENST00000641236.1:n.202G=
ENST00000641319.1:c.190G= ENSP00000493128.1:p.Gly64=
ENST00000641471.1:c.277G= ENSP00000493146.1:p.Gly93=
ENST00000641548.1:c.*42G= ENSP00000492984.1:n.*42G=
ENST00000641691.1:c.*42G= ENSP00000492910.1:n.*42G=
ENST00000641924.1:c.124+4673G= ENSP00000493063.1:n.124+4673G=
ENST00000642050.2:c.190G= MANE Select ENSP00000493153.1:p.Gly64=
ENST00000372779.8:c.277G= ENSP00000361865.4:p.Gly93=
ENST00000433473.7:c.190G= ENSP00000394863.3:p.Gly64=
ENST00000449045.6:c.125-2930G= ENSP00000392293.2:n.125-2930G=
ENST00000526547.1:c.40G= ENSP00000436481.1:p.Gly14=
ENST00000527311.6:c.125-385G= ENSP00000436695.2:n.125-385G=
ENST00000529905.5:c.190G= ENSP00000432053.1:p.Gly64=
ENST00000530704.5:c.190G= ENSP00000431655.1:p.Gly64=
NM_000310.3:c.190G= , LRG_690t1:c.190G= NP_000301.1:p.Gly64=
NM_001142604.1:c.125-2930G= NP_001136076.1:n.125-2930G=
XM_005271008.1:c.190G= XP_005271065.1:p.Gly64=
NM_001363695.1:c.190G= NP_001350624.1:p.Gly64=
NM_000310.4:c.190G= MANE Select NP_000301.1:p.Gly64=
NM_001142604.2:c.125-2930G= NP_001136076.1:n.125-2930G=
NM_001363695.2:c.190G= NP_001350624.1:p.Gly64=