Canonical Allele Identifier: CA1144048711
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097220G= , CM000663.2:g.40097220G= GRCh38
NC_000001.10:g.40562892G= , CM000663.1:g.40562892G= GRCh37
NC_000001.9:g.40335479G= NCBI36
NG_009192.1:g.5251C= , LRG_690:g.5251C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.19C= ENSP00000361865.5:p.Leu7=
ENST00000433473.8:c.19C= ENSP00000394863.4:p.Leu7=
ENST00000439754.6:c.19C= ENSP00000403207.2:p.Leu7=
ENST00000449045.7:c.19C= ENSP00000392293.2:p.Leu7=
ENST00000527311.7:c.19C= ENSP00000436695.3:p.Leu7=
ENST00000530704.6:c.19C= ENSP00000431655.1:p.Leu7=
ENST00000641236.1:n.31C=
ENST00000641319.1:c.19C= ENSP00000493128.1:p.Leu7=
ENST00000641471.1:c.19C= ENSP00000493146.1:p.Leu7=
ENST00000641548.1:c.19C= ENSP00000492984.1:p.Leu7=
ENST00000641691.1:c.19C= ENSP00000492910.1:p.Leu7=
ENST00000641924.1:c.19C= ENSP00000493063.1:p.Leu7=
ENST00000642050.2:c.19C= MANE Select ENSP00000493153.1:p.Leu7=
ENST00000372779.8:c.19C= ENSP00000361865.4:p.Leu7=
ENST00000433473.7:c.19C= ENSP00000394863.3:p.Leu7=
ENST00000449045.6:c.19C= ENSP00000392293.2:p.Leu7=
ENST00000527311.6:c.19C= ENSP00000436695.2:p.Leu7=
ENST00000529905.5:c.19C= ENSP00000432053.1:p.Leu7=
ENST00000530704.5:c.19C= ENSP00000431655.1:p.Leu7=
NM_000310.3:c.19C= , LRG_690t1:c.19C= NP_000301.1:p.Leu7=
NM_001142604.1:c.19C= NP_001136076.1:p.Leu7=
XM_005271008.1:c.19C= XP_005271065.1:p.Leu7=
NM_001363695.1:c.19C= NP_001350624.1:p.Leu7=
NM_000310.4:c.19C= MANE Select NP_000301.1:p.Leu7=
NM_001142604.2:c.19C= NP_001136076.1:p.Leu7=
NM_001363695.2:c.19C= NP_001350624.1:p.Leu7=