Canonical Allele Identifier: CA1164245540
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078638C= , CM000663.2:g.40078638C= GRCh38
NC_000001.10:g.40544310C= , CM000663.1:g.40544310C= GRCh37
NC_000001.9:g.40316897C= NCBI36
NG_009192.1:g.23833G= , LRG_690:g.23833G=

Transcript Alleles

HGVS Amino-acid change
ENST00000433473.8:c.645G= ENSP00000394863.4:p.Lys215=
ENST00000439754.6:c.648G= ENSP00000403207.2:p.Lys216=
ENST00000449045.7:c.339G= ENSP00000392293.2:p.Lys113=
ENST00000527311.7:c.417G= ENSP00000436695.3:p.Lys139=
ENST00000530076.6:c.-10G= ENSP00000434007.1:n.-10G=
ENST00000530704.6:c.*271G= ENSP00000431655.1:n.*271G=
ENST00000641083.1:c.626G=
ENST00000641236.1:n.885G=
ENST00000641319.1:c.648G= ENSP00000493128.1:p.Lys216=
ENST00000641381.1:c.149-1725G=
ENST00000641471.1:c.735G= ENSP00000493146.1:p.Lys245=
ENST00000641691.1:c.*500G= ENSP00000492910.1:n.*500G=
ENST00000641924.1:c.*77G= ENSP00000493063.1:n.*77G=
ENST00000642050.2:c.648G= MANE Select ENSP00000493153.1:p.Lys216=
ENST00000372775.2:n.45G=
ENST00000372779.8:c.735G= ENSP00000361865.4:p.Lys245=
ENST00000433473.7:c.648G= ENSP00000394863.3:p.Lys216=
ENST00000439754.5:c.333G= ENSP00000403207.1:p.Lys111=
ENST00000449045.6:c.339G= ENSP00000392293.2:p.Lys113=
ENST00000527311.6:c.423G= ENSP00000436695.2:p.Lys141=
ENST00000529905.5:c.648G= ENSP00000432053.1:p.Lys216=
ENST00000530076.5:c.-10G= ENSP00000434007.1:n.-10G=
ENST00000530704.5:c.*271G= ENSP00000431655.1:n.*271G=
NM_000310.3:c.648G= , LRG_690t1:c.648G= NP_000301.1:p.Lys216=
NM_001142604.1:c.339G= NP_001136076.1:p.Lys113=
XM_005271008.1:c.648G= XP_005271065.1:p.Lys216=
NM_001363695.1:c.648G= NP_001350624.1:p.Lys216=
NM_000310.4:c.648G= MANE Select NP_000301.1:p.Lys216=
NM_001142604.2:c.339G= NP_001136076.1:p.Lys113=
NM_001363695.2:c.648G= NP_001350624.1:p.Lys216=