Canonical Allele Identifier: CA339845308
Gene: PPT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40074071A>G , CM000663.2:g.40074071A>G GRCh38
NC_000001.10:g.40539743A>G , CM000663.1:g.40539743A>G GRCh37
NC_000001.9:g.40312330A>G NCBI36
NG_009192.1:g.28400T>C , LRG_690:g.28400T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.908T>C ENSP00000394863.4:p.Phe303Ser
ENST00000439754.6:c.839T>C ENSP00000403207.2:p.Phe280Ser
ENST00000449045.7:c.602T>C ENSP00000392293.2:p.Phe201Ser
ENST00000530076.6:c.254T>C ENSP00000434007.1:p.Phe85Ser
ENST00000530704.6:c.*534T>C ENSP00000431655.1:n.*534T>C
ENST00000641083.1:c.1001T>C
ENST00000641236.1:n.1148T>C
ENST00000641319.1:c.*121T>C ENSP00000493128.1:n.*121T>C
ENST00000641381.1:c.333T>C
ENST00000641471.1:c.998T>C ENSP00000493146.1:p.Phe333Ser
ENST00000641691.1:c.*763T>C ENSP00000492910.1:n.*763T>C
ENST00000641924.1:c.*340T>C ENSP00000493063.1:n.*340T>C
ENST00000642050.2:c.911T>C MANE Select ENSP00000493153.1:p.Phe304Ser
ENST00000372775.2:n.308T>C
ENST00000433473.7:c.911T>C ENSP00000394863.3:p.Phe304Ser
ENST00000439754.5:c.524T>C ENSP00000403207.1:p.Phe175Ser
ENST00000449045.6:c.602T>C ENSP00000392293.2:p.Phe201Ser
ENST00000529905.5:c.911T>C ENSP00000432053.1:p.Phe304Ser
ENST00000530076.5:c.254T>C ENSP00000434007.1:p.Phe85Ser
ENST00000530704.5:c.*534T>C ENSP00000431655.1:n.*534T>C
NM_000310.3:c.911T>C , LRG_690t1:c.911T>C NP_000301.1:p.Phe304Ser
NM_001142604.1:c.602T>C NP_001136076.1:p.Phe201Ser
XM_005271008.1:c.839T>C XP_005271065.1:p.Phe280Ser
NM_001363695.1:c.839T>C NP_001350624.1:p.Phe280Ser
NM_000310.4:c.911T>C MANE Select NP_000301.1:p.Phe304Ser
NM_001142604.2:c.602T>C NP_001136076.1:p.Phe201Ser
NM_001363695.2:c.839T>C NP_001350624.1:p.Phe280Ser