Canonical Allele Identifier: CA339848853
Gene: PPT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40091357A>T , CM000663.2:g.40091357A>T GRCh38
NC_000001.10:g.40557029A>T , CM000663.1:g.40557029A>T GRCh37
NC_000001.9:g.40329616A>T NCBI36
NG_009192.1:g.11114T>A , LRG_690:g.11114T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372779.9:c.*241T>A ENSP00000361865.5:n.*241T>A
ENST00000433473.8:c.402T>A ENSP00000394863.4:p.Asn134Lys
ENST00000439754.6:c.405T>A ENSP00000403207.2:p.Asn135Lys
ENST00000449045.7:c.125-1845T>A ENSP00000392293.2:n.125-1845T>A
ENST00000526547.2:c.685T>A
ENST00000527311.7:c.277T>A ENSP00000436695.3:p.Ser93Thr
ENST00000530704.6:c.405T>A ENSP00000431655.1:p.Asn135Lys
ENST00000641083.1:c.383T>A
ENST00000641236.1:n.642T>A
ENST00000641319.1:c.405T>A ENSP00000493128.1:p.Asn135Lys
ENST00000641381.1:c.17T>A
ENST00000641471.1:c.492T>A ENSP00000493146.1:p.Asn164Lys
ENST00000641548.1:c.*257T>A ENSP00000492984.1:n.*257T>A
ENST00000641691.1:c.*257T>A ENSP00000492910.1:n.*257T>A
ENST00000641924.1:c.124+5758T>A ENSP00000493063.1:n.124+5758T>A
ENST00000642050.2:c.405T>A MANE Select ENSP00000493153.1:p.Asn135Lys
ENST00000372779.8:c.492T>A ENSP00000361865.4:p.Asn164Lys
ENST00000433473.7:c.405T>A ENSP00000394863.3:p.Asn135Lys
ENST00000439754.5:c.90T>A ENSP00000403207.1:p.Asn30Lys
ENST00000449045.6:c.125-1845T>A ENSP00000392293.2:n.125-1845T>A
ENST00000526547.1:c.255T>A ENSP00000436481.1:p.Asn85Lys
ENST00000527311.6:c.180T>A ENSP00000436695.2:p.Asn60Lys
ENST00000529905.5:c.405T>A ENSP00000432053.1:p.Asn135Lys
ENST00000530704.5:c.405T>A ENSP00000431655.1:p.Asn135Lys
NM_000310.3:c.405T>A , LRG_690t1:c.405T>A NP_000301.1:p.Asn135Lys
NM_001142604.1:c.125-1845T>A NP_001136076.1:n.125-1845T>A
XM_005271008.1:c.405T>A XP_005271065.1:p.Asn135Lys
NM_001363695.1:c.405T>A NP_001350624.1:p.Asn135Lys
NM_000310.4:c.405T>A MANE Select NP_000301.1:p.Asn135Lys
NM_001142604.2:c.125-1845T>A NP_001136076.1:n.125-1845T>A
NM_001363695.2:c.405T>A NP_001350624.1:p.Asn135Lys