Canonical Allele Identifier: CA1164245536
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078629C= , CM000663.2:g.40078629C= GRCh38
NC_000001.10:g.40544301C= , CM000663.1:g.40544301C= GRCh37
NC_000001.9:g.40316888C= NCBI36
NG_009192.1:g.23842G= , LRG_690:g.23842G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.654G= ENSP00000394863.4:p.Leu218=
ENST00000439754.6:c.657G= ENSP00000403207.2:p.Leu219=
ENST00000449045.7:c.348G= ENSP00000392293.2:p.Leu116=
ENST00000527311.7:c.426G= ENSP00000436695.3:p.Leu142=
ENST00000530076.6:c.-1G= ENSP00000434007.1:n.-1G=
ENST00000530704.6:c.*280G= ENSP00000431655.1:n.*280G=
ENST00000641083.1:c.635G=
ENST00000641236.1:n.894G=
ENST00000641319.1:c.657G= ENSP00000493128.1:p.Leu219=
ENST00000641381.1:c.149-1716G=
ENST00000641471.1:c.744G= ENSP00000493146.1:p.Leu248=
ENST00000641691.1:c.*509G= ENSP00000492910.1:n.*509G=
ENST00000641924.1:c.*86G= ENSP00000493063.1:n.*86G=
ENST00000642050.2:c.657G= MANE Select ENSP00000493153.1:p.Leu219=
ENST00000372775.2:n.54G=
ENST00000372779.8:c.744G= ENSP00000361865.4:p.Leu248=
ENST00000433473.7:c.657G= ENSP00000394863.3:p.Leu219=
ENST00000439754.5:c.342G= ENSP00000403207.1:p.Leu114=
ENST00000449045.6:c.348G= ENSP00000392293.2:p.Leu116=
ENST00000527311.6:c.432G= ENSP00000436695.2:p.Leu144=
ENST00000529905.5:c.657G= ENSP00000432053.1:p.Leu219=
ENST00000530076.5:c.-1G= ENSP00000434007.1:n.-1G=
ENST00000530704.5:c.*280G= ENSP00000431655.1:n.*280G=
NM_000310.3:c.657G= , LRG_690t1:c.657G= NP_000301.1:p.Leu219=
NM_001142604.1:c.348G= NP_001136076.1:p.Leu116=
XM_005271008.1:c.657G= XP_005271065.1:p.Leu219=
NM_001363695.1:c.657G= NP_001350624.1:p.Leu219=
NM_000310.4:c.657G= MANE Select NP_000301.1:p.Leu219=
NM_001142604.2:c.348G= NP_001136076.1:p.Leu116=
NM_001363695.2:c.657G= NP_001350624.1:p.Leu219=