Canonical Allele Identifier: CA1164245544
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078641G= , CM000663.2:g.40078641G= GRCh38
NC_000001.10:g.40544313G= , CM000663.1:g.40544313G= GRCh37
NC_000001.9:g.40316900G= NCBI36
NG_009192.1:g.23830C= , LRG_690:g.23830C=

Transcript Alleles

HGVS Amino-acid change
ENST00000433473.8:c.642C= ENSP00000394863.4:p.Tyr214=
ENST00000439754.6:c.645C= ENSP00000403207.2:p.Tyr215=
ENST00000449045.7:c.336C= ENSP00000392293.2:p.Tyr112=
ENST00000527311.7:c.414C= ENSP00000436695.3:p.Tyr138=
ENST00000530076.6:c.-13C= ENSP00000434007.1:n.-13C=
ENST00000530704.6:c.*268C= ENSP00000431655.1:n.*268C=
ENST00000641083.1:c.623C=
ENST00000641236.1:n.882C=
ENST00000641319.1:c.645C= ENSP00000493128.1:p.Tyr215=
ENST00000641381.1:c.149-1728C=
ENST00000641471.1:c.732C= ENSP00000493146.1:p.Tyr244=
ENST00000641691.1:c.*497C= ENSP00000492910.1:n.*497C=
ENST00000641924.1:c.*74C= ENSP00000493063.1:n.*74C=
ENST00000642050.2:c.645C= MANE Select ENSP00000493153.1:p.Tyr215=
ENST00000372775.2:n.42C=
ENST00000372779.8:c.732C= ENSP00000361865.4:p.Tyr244=
ENST00000433473.7:c.645C= ENSP00000394863.3:p.Tyr215=
ENST00000439754.5:c.330C= ENSP00000403207.1:p.Tyr110=
ENST00000449045.6:c.336C= ENSP00000392293.2:p.Tyr112=
ENST00000527311.6:c.420C= ENSP00000436695.2:p.Tyr140=
ENST00000529905.5:c.645C= ENSP00000432053.1:p.Tyr215=
ENST00000530076.5:c.-13C= ENSP00000434007.1:n.-13C=
ENST00000530704.5:c.*268C= ENSP00000431655.1:n.*268C=
NM_000310.3:c.645C= , LRG_690t1:c.645C= NP_000301.1:p.Tyr215=
NM_001142604.1:c.336C= NP_001136076.1:p.Tyr112=
XM_005271008.1:c.645C= XP_005271065.1:p.Tyr215=
NM_001363695.1:c.645C= NP_001350624.1:p.Tyr215=
NM_000310.4:c.645C= MANE Select NP_000301.1:p.Tyr215=
NM_001142604.2:c.336C= NP_001136076.1:p.Tyr112=
NM_001363695.2:c.645C= NP_001350624.1:p.Tyr215=