Canonical Allele Identifier: CA1164243725

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074390_40074393delinsCTTT , CM000663.2:g.40074390_40074393delinsCTTT	GRCh38
NC_000001.10:g.40540062_40540065delinsCTTT , CM000663.1:g.40540062_40540065delinsCTTT	GRCh37
NC_000001.9:g.40312649_40312652delinsCTTT	NCBI36
NG_009192.1:g.28078_28081delinsAAAG , LRG_690:g.28078_28081delinsAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.796-210_796-207delinsAAAG	ENSP00000394863.4:n.796-210_796-207delinsAAAG
ENST00000439754.6:c.727-210_727-207delinsAAAG	ENSP00000403207.2:n.727-210_727-207delinsAAAG
ENST00000449045.7:c.490-210_490-207delinsAAAG	ENSP00000392293.2:n.490-210_490-207delinsAAAG
ENST00000527311.7:c.568-210_568-207delinsAAAG	ENSP00000436695.3:n.568-210_568-207delinsAAAG
ENST00000530076.6:c.142-210_142-207delinsAAAG	ENSP00000434007.1:n.142-210_142-207delinsAAAG
ENST00000530704.6:c.*422-210_*422-207delinsAAAG	ENSP00000431655.1:n.*422-210_*422-207delinsAAAG
ENST00000641083.1:c.889-210_889-207delinsAAAG
ENST00000641236.1:n.1036-210_1036-207delinsAAAG
ENST00000641319.1:c.*9-210_*9-207delinsAAAG	ENSP00000493128.1:n.*9-210_*9-207delinsAAAG
ENST00000641381.1:c.221-210_221-207delinsAAAG
ENST00000641471.1:c.886-210_886-207delinsAAAG	ENSP00000493146.1:n.886-210_886-207delinsAAAG
ENST00000641691.1:c.*651-210_*651-207delinsAAAG	ENSP00000492910.1:n.*651-210_*651-207delinsAAAG
ENST00000641924.1:c.*228-210_*228-207delinsAAAG	ENSP00000493063.1:n.*228-210_*228-207delinsAAAG
ENST00000642050.2:c.799-210_799-207delinsAAAG MANE Select	ENSP00000493153.1:n.799-210_799-207delinsAAAG
ENST00000372775.2:n.196-210_196-207delinsAAAG
ENST00000433473.7:c.799-210_799-207delinsAAAG	ENSP00000394863.3:n.799-210_799-207delinsAAAG
ENST00000439754.5:c.412-210_412-207delinsAAAG	ENSP00000403207.1:n.412-210_412-207delinsAAAG
ENST00000449045.6:c.490-210_490-207delinsAAAG	ENSP00000392293.2:n.490-210_490-207delinsAAAG
ENST00000527311.6:c.574-210_574-207delinsAAAG	ENSP00000436695.2:n.574-210_574-207delinsAAAG
ENST00000529905.5:c.799-210_799-207delinsAAAG	ENSP00000432053.1:n.799-210_799-207delinsAAAG
ENST00000530076.5:c.142-210_142-207delinsAAAG	ENSP00000434007.1:n.142-210_142-207delinsAAAG
ENST00000530704.5:c.*422-210_*422-207delinsAAAG	ENSP00000431655.1:n.*422-210_*422-207delinsAAAG
NM_000310.3:c.799-210_799-207delinsAAAG , LRG_690t1:c.799-210_799-207delinsAAAG	NP_000301.1:n.799-210_799-207delinsAAAG
NM_001142604.1:c.490-210_490-207delinsAAAG	NP_001136076.1:n.490-210_490-207delinsAAAG
XM_005271008.1:c.727-210_727-207delinsAAAG	XP_005271065.1:n.727-210_727-207delinsAAAG
NM_001363695.1:c.727-210_727-207delinsAAAG	NP_001350624.1:n.727-210_727-207delinsAAAG
NM_000310.4:c.799-210_799-207delinsAAAG MANE Select	NP_000301.1:n.799-210_799-207delinsAAAG
NM_001142604.2:c.490-210_490-207delinsAAAG	NP_001136076.1:n.490-210_490-207delinsAAAG
NM_001363695.2:c.727-210_727-207delinsAAAG	NP_001350624.1:n.727-210_727-207delinsAAAG