Canonical Allele Identifier: CA1164252320

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092149_40092152delinsCAAG , CM000663.2:g.40092149_40092152delinsCAAG	GRCh38
NC_000001.10:g.40557821_40557824delinsCAAG , CM000663.1:g.40557821_40557824delinsCAAG	GRCh37
NC_000001.9:g.40330408_40330411delinsCAAG	NCBI36
NG_009192.1:g.10319_10322delinsCTTG , LRG_690:g.10319_10322delinsCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*91_*94delinsCTTG	ENSP00000361865.5:n.*91_*94delinsCTTG
ENST00000433473.8:c.252_255delinsCTTG	ENSP00000394863.4:p.Phe84=
ENST00000439754.6:c.255_258delinsCTTG	ENSP00000403207.2:p.Phe85=
ENST00000449045.7:c.125-2640_125-2637delinsCTTG	ENSP00000392293.2:n.125-2640_125-2637delinsCTTG
ENST00000526547.2:c.535_538delinsCTTG
ENST00000527311.7:c.234+246_234+249delinsCTTG	ENSP00000436695.3:n.234+246_234+249delinsCTTG
ENST00000530704.6:c.255_258delinsCTTG	ENSP00000431655.1:p.Phe85=
ENST00000641083.1:c.233_236delinsCTTG
ENST00000641236.1:n.492_495delinsCTTG
ENST00000641319.1:c.255_258delinsCTTG	ENSP00000493128.1:p.Phe85=
ENST00000641471.1:c.342_345delinsCTTG	ENSP00000493146.1:p.Phe114=
ENST00000641548.1:c.*107_*110delinsCTTG	ENSP00000492984.1:n.*107_*110delinsCTTG
ENST00000641691.1:c.*107_*110delinsCTTG	ENSP00000492910.1:n.*107_*110delinsCTTG
ENST00000641924.1:c.124+4963_124+4966delinsCTTG	ENSP00000493063.1:n.124+4963_124+4966delinsCTTG
ENST00000642050.2:c.255_258delinsCTTG MANE Select	ENSP00000493153.1:p.Phe85=
ENST00000372779.8:c.342_345delinsCTTG	ENSP00000361865.4:p.Phe114=
ENST00000433473.7:c.255_258delinsCTTG	ENSP00000394863.3:p.Phe85=
ENST00000449045.6:c.125-2640_125-2637delinsCTTG	ENSP00000392293.2:n.125-2640_125-2637delinsCTTG
ENST00000526547.1:c.105_108delinsCTTG	ENSP00000436481.1:p.Phe35=
ENST00000527311.6:c.125-95_125-92delinsCTTG	ENSP00000436695.2:n.125-95_125-92delinsCTTG
ENST00000529905.5:c.255_258delinsCTTG	ENSP00000432053.1:p.Phe85=
ENST00000530704.5:c.255_258delinsCTTG	ENSP00000431655.1:p.Phe85=
NM_000310.3:c.255_258delinsCTTG , LRG_690t1:c.255_258delinsCTTG	NP_000301.1:p.Phe85=
NM_001142604.1:c.125-2640_125-2637delinsCTTG	NP_001136076.1:n.125-2640_125-2637delinsCTTG
XM_005271008.1:c.255_258delinsCTTG	XP_005271065.1:p.Phe85=
NM_001363695.1:c.255_258delinsCTTG	NP_001350624.1:p.Phe85=
NM_000310.4:c.255_258delinsCTTG MANE Select	NP_000301.1:p.Phe85=
NM_001142604.2:c.125-2640_125-2637delinsCTTG	NP_001136076.1:n.125-2640_125-2637delinsCTTG
NM_001363695.2:c.255_258delinsCTTG	NP_001350624.1:p.Phe85=