Canonical Allele Identifier: CA1164245523
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078571C= , CM000663.2:g.40078571C= GRCh38
NC_000001.10:g.40544243C= , CM000663.1:g.40544243C= GRCh37
NC_000001.9:g.40316830C= NCBI36
NG_009192.1:g.23900G= , LRG_690:g.23900G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.8:c.712G= ENSP00000394863.4:p.Val238=
ENST00000439754.6:c.715G= ENSP00000403207.2:p.Val239=
ENST00000449045.7:c.406G= ENSP00000392293.2:p.Val136=
ENST00000527311.7:c.484G= ENSP00000436695.3:p.Val162=
ENST00000530076.6:c.58G= ENSP00000434007.1:p.Val20=
ENST00000530704.6:c.*338G= ENSP00000431655.1:n.*338G=
ENST00000641083.1:c.693G=
ENST00000641236.1:n.952G=
ENST00000641319.1:c.715G= ENSP00000493128.1:p.Val239=
ENST00000641381.1:c.149-1658G=
ENST00000641471.1:c.802G= ENSP00000493146.1:p.Val268=
ENST00000641691.1:c.*567G= ENSP00000492910.1:n.*567G=
ENST00000641924.1:c.*144G= ENSP00000493063.1:n.*144G=
ENST00000642050.2:c.715G= MANE Select ENSP00000493153.1:p.Val239=
ENST00000372775.2:n.112G=
ENST00000372779.8:c.802G= ENSP00000361865.4:p.Val268=
ENST00000433473.7:c.715G= ENSP00000394863.3:p.Val239=
ENST00000439754.5:c.400G= ENSP00000403207.1:p.Val134=
ENST00000449045.6:c.406G= ENSP00000392293.2:p.Val136=
ENST00000527311.6:c.490G= ENSP00000436695.2:p.Val164=
ENST00000529905.5:c.715G= ENSP00000432053.1:p.Val239=
ENST00000530076.5:c.58G= ENSP00000434007.1:p.Val20=
ENST00000530704.5:c.*338G= ENSP00000431655.1:n.*338G=
NM_000310.3:c.715G= , LRG_690t1:c.715G= NP_000301.1:p.Val239=
NM_001142604.1:c.406G= NP_001136076.1:p.Val136=
XM_005271008.1:c.715G= XP_005271065.1:p.Val239=
NM_001363695.1:c.715G= NP_001350624.1:p.Val239=
NM_000310.4:c.715G= MANE Select NP_000301.1:p.Val239=
NM_001142604.2:c.406G= NP_001136076.1:p.Val136=
NM_001363695.2:c.715G= NP_001350624.1:p.Val239=