Canonical Allele Identifier: CA1164243567
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40074154A= , CM000663.2:g.40074154A= GRCh38
NC_000001.10:g.40539826A= , CM000663.1:g.40539826A= GRCh37
NC_000001.9:g.40312413A= NCBI36
NG_009192.1:g.28317T= , LRG_690:g.28317T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.825T= ENSP00000394863.4:p.Asn275=
ENST00000439754.6:c.756T= ENSP00000403207.2:p.Asn252=
ENST00000449045.7:c.519T= ENSP00000392293.2:p.Asn173=
ENST00000527311.7:c.597T= ENSP00000436695.3:p.Asn199=
ENST00000530076.6:c.171T= ENSP00000434007.1:p.Asn57=
ENST00000530704.6:c.*451T= ENSP00000431655.1:n.*451T=
ENST00000641083.1:c.918T=
ENST00000641236.1:n.1065T=
ENST00000641319.1:c.*38T= ENSP00000493128.1:n.*38T=
ENST00000641381.1:c.250T=
ENST00000641471.1:c.915T= ENSP00000493146.1:p.Asn305=
ENST00000641691.1:c.*680T= ENSP00000492910.1:n.*680T=
ENST00000641924.1:c.*257T= ENSP00000493063.1:n.*257T=
ENST00000642050.2:c.828T= MANE Select ENSP00000493153.1:p.Asn276=
ENST00000372775.2:n.225T=
ENST00000433473.7:c.828T= ENSP00000394863.3:p.Asn276=
ENST00000439754.5:c.441T= ENSP00000403207.1:p.Asn147=
ENST00000449045.6:c.519T= ENSP00000392293.2:p.Asn173=
ENST00000527311.6:c.603T= ENSP00000436695.2:p.Asn201=
ENST00000529905.5:c.828T= ENSP00000432053.1:p.Asn276=
ENST00000530076.5:c.171T= ENSP00000434007.1:p.Asn57=
ENST00000530704.5:c.*451T= ENSP00000431655.1:n.*451T=
NM_000310.3:c.828T= , LRG_690t1:c.828T= NP_000301.1:p.Asn276=
NM_001142604.1:c.519T= NP_001136076.1:p.Asn173=
XM_005271008.1:c.756T= XP_005271065.1:p.Asn252=
NM_001363695.1:c.756T= NP_001350624.1:p.Asn252=
NM_000310.4:c.828T= MANE Select NP_000301.1:p.Asn276=
NM_001142604.2:c.519T= NP_001136076.1:p.Asn173=
NM_001363695.2:c.756T= NP_001350624.1:p.Asn252=