Canonical Allele Identifier: CA1144228758
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097114C= , CM000663.2:g.40097114C= GRCh38
NC_000001.10:g.40562786C= , CM000663.1:g.40562786C= GRCh37
NC_000001.9:g.40335373C= NCBI36
NG_009192.1:g.5357G= , LRG_690:g.5357G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.125G= ENSP00000361865.5:p.Gly42=
ENST00000433473.8:c.124+1G= ENSP00000394863.4:n.124+1G=
ENST00000439754.6:c.124+1G= ENSP00000403207.2:n.124+1G=
ENST00000449045.7:c.124+1G= ENSP00000392293.2:n.124+1G=
ENST00000526547.2:c.99G=
ENST00000527311.7:c.124+1G= ENSP00000436695.3:n.124+1G=
ENST00000530704.6:c.124+1G= ENSP00000431655.1:n.124+1G=
ENST00000641083.1:c.102+1G=
ENST00000641236.1:n.136+1G=
ENST00000641319.1:c.124+1G= ENSP00000493128.1:n.124+1G=
ENST00000641471.1:c.124+1G= ENSP00000493146.1:n.124+1G=
ENST00000641548.1:c.124+1G= ENSP00000492984.1:n.124+1G=
ENST00000641691.1:c.124+1G= ENSP00000492910.1:n.124+1G=
ENST00000641924.1:c.124+1G= ENSP00000493063.1:n.124+1G=
ENST00000642050.2:c.124+1G= MANE Select ENSP00000493153.1:n.124+1G=
ENST00000372779.8:c.124+1G= ENSP00000361865.4:n.124+1G=
ENST00000433473.7:c.124+1G= ENSP00000394863.3:n.124+1G=
ENST00000449045.6:c.124+1G= ENSP00000392293.2:n.124+1G=
ENST00000527311.6:c.124+1G= ENSP00000436695.2:n.124+1G=
ENST00000529905.5:c.124+1G= ENSP00000432053.1:n.124+1G=
ENST00000530704.5:c.124+1G= ENSP00000431655.1:n.124+1G=
NM_000310.3:c.124+1G= , LRG_690t1:c.124+1G= NP_000301.1:n.124+1G=
NM_001142604.1:c.124+1G= NP_001136076.1:n.124+1G=
XM_005271008.1:c.124+1G= XP_005271065.1:n.124+1G=
NM_001363695.1:c.124+1G= NP_001350624.1:n.124+1G=
NM_000310.4:c.124+1G= MANE Select NP_000301.1:n.124+1G=
NM_001142604.2:c.124+1G= NP_001136076.1:n.124+1G=
NM_001363695.2:c.124+1G= NP_001350624.1:n.124+1G=