Canonical Allele Identifier: CA1144228759
Gene: PPT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078642T= , CM000663.2:g.40078642T= GRCh38
NC_000001.10:g.40544314T= , CM000663.1:g.40544314T= GRCh37
NC_000001.9:g.40316901T= NCBI36
NG_009192.1:g.23829A= , LRG_690:g.23829A=

Transcript Alleles

HGVS Amino-acid change
ENST00000433473.8:c.641A= ENSP00000394863.4:p.Tyr214=
ENST00000439754.6:c.644A= ENSP00000403207.2:p.Tyr215=
ENST00000449045.7:c.335A= ENSP00000392293.2:p.Tyr112=
ENST00000527311.7:c.413A= ENSP00000436695.3:p.Tyr138=
ENST00000530076.6:c.-14A= ENSP00000434007.1:n.-14A=
ENST00000530704.6:c.*267A= ENSP00000431655.1:n.*267A=
ENST00000641083.1:c.622A=
ENST00000641236.1:n.881A=
ENST00000641319.1:c.644A= ENSP00000493128.1:p.Tyr215=
ENST00000641381.1:c.149-1729A=
ENST00000641471.1:c.731A= ENSP00000493146.1:p.Tyr244=
ENST00000641691.1:c.*496A= ENSP00000492910.1:n.*496A=
ENST00000641924.1:c.*73A= ENSP00000493063.1:n.*73A=
ENST00000642050.2:c.644A= MANE Select ENSP00000493153.1:p.Tyr215=
ENST00000372775.2:n.41A=
ENST00000372779.8:c.731A= ENSP00000361865.4:p.Tyr244=
ENST00000433473.7:c.644A= ENSP00000394863.3:p.Tyr215=
ENST00000439754.5:c.329A= ENSP00000403207.1:p.Tyr110=
ENST00000449045.6:c.335A= ENSP00000392293.2:p.Tyr112=
ENST00000527311.6:c.419A= ENSP00000436695.2:p.Tyr140=
ENST00000529905.5:c.644A= ENSP00000432053.1:p.Tyr215=
ENST00000530076.5:c.-14A= ENSP00000434007.1:n.-14A=
ENST00000530704.5:c.*267A= ENSP00000431655.1:n.*267A=
NM_000310.3:c.644A= , LRG_690t1:c.644A= NP_000301.1:p.Tyr215=
NM_001142604.1:c.335A= NP_001136076.1:p.Tyr112=
XM_005271008.1:c.644A= XP_005271065.1:p.Tyr215=
NM_001363695.1:c.644A= NP_001350624.1:p.Tyr215=
NM_000310.4:c.644A= MANE Select NP_000301.1:p.Tyr215=
NM_001142604.2:c.335A= NP_001136076.1:p.Tyr112=
NM_001363695.2:c.644A= NP_001350624.1:p.Tyr215=