Canonical Allele Identifier: CA1164245542
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078640T= , CM000663.2:g.40078640T= GRCh38
NC_000001.10:g.40544312T= , CM000663.1:g.40544312T= GRCh37
NC_000001.9:g.40316899T= NCBI36
NG_009192.1:g.23831A= , LRG_690:g.23831A=

Transcript Alleles

HGVS Amino-acid change
ENST00000433473.8:c.643A= ENSP00000394863.4:p.Lys215=
ENST00000439754.6:c.646A= ENSP00000403207.2:p.Lys216=
ENST00000449045.7:c.337A= ENSP00000392293.2:p.Lys113=
ENST00000527311.7:c.415A= ENSP00000436695.3:p.Lys139=
ENST00000530076.6:c.-12A= ENSP00000434007.1:n.-12A=
ENST00000530704.6:c.*269A= ENSP00000431655.1:n.*269A=
ENST00000641083.1:c.624A=
ENST00000641236.1:n.883A=
ENST00000641319.1:c.646A= ENSP00000493128.1:p.Lys216=
ENST00000641381.1:c.149-1727A=
ENST00000641471.1:c.733A= ENSP00000493146.1:p.Lys245=
ENST00000641691.1:c.*498A= ENSP00000492910.1:n.*498A=
ENST00000641924.1:c.*75A= ENSP00000493063.1:n.*75A=
ENST00000642050.2:c.646A= MANE Select ENSP00000493153.1:p.Lys216=
ENST00000372775.2:n.43A=
ENST00000372779.8:c.733A= ENSP00000361865.4:p.Lys245=
ENST00000433473.7:c.646A= ENSP00000394863.3:p.Lys216=
ENST00000439754.5:c.331A= ENSP00000403207.1:p.Lys111=
ENST00000449045.6:c.337A= ENSP00000392293.2:p.Lys113=
ENST00000527311.6:c.421A= ENSP00000436695.2:p.Lys141=
ENST00000529905.5:c.646A= ENSP00000432053.1:p.Lys216=
ENST00000530076.5:c.-12A= ENSP00000434007.1:n.-12A=
ENST00000530704.5:c.*269A= ENSP00000431655.1:n.*269A=
NM_000310.3:c.646A= , LRG_690t1:c.646A= NP_000301.1:p.Lys216=
NM_001142604.1:c.337A= NP_001136076.1:p.Lys113=
XM_005271008.1:c.646A= XP_005271065.1:p.Lys216=
NM_001363695.1:c.646A= NP_001350624.1:p.Lys216=
NM_000310.4:c.646A= MANE Select NP_000301.1:p.Lys216=
NM_001142604.2:c.337A= NP_001136076.1:p.Lys113=
NM_001363695.2:c.646A= NP_001350624.1:p.Lys216=