Canonical Allele Identifier: CA2743276826

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40078743_40078744insAC , CM000663.2:g.40078743_40078744insAC	GRCh38
NC_000001.10:g.40544415_40544416insAC , CM000663.1:g.40544415_40544416insAC	GRCh37
NC_000001.9:g.40317002_40317003insAC	NCBI36
NG_009192.1:g.23727_23728insGT , LRG_690:g.23727_23728insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.625-86_625-85insGT	ENSP00000394863.4:n.625-86_625-85insGT
ENST00000439754.6:c.628-86_628-85insGT	ENSP00000403207.2:n.628-86_628-85insGT
ENST00000449045.7:c.319-86_319-85insGT	ENSP00000392293.2:n.319-86_319-85insGT
ENST00000527311.7:c.397-86_397-85insGT	ENSP00000436695.3:n.397-86_397-85insGT
ENST00000530076.6:c.-30-86_-30-85insGT	ENSP00000434007.1:n.-30-86_-30-85insGT
ENST00000530704.6:c.*251-86_*251-85insGT	ENSP00000431655.1:n.*251-86_*251-85insGT
ENST00000641083.1:c.606-86_606-85insGT
ENST00000641236.1:n.865-86_865-85insGT
ENST00000641319.1:c.628-86_628-85insGT	ENSP00000493128.1:n.628-86_628-85insGT
ENST00000641381.1:c.149-1831_149-1830insGT
ENST00000641471.1:c.715-86_715-85insGT	ENSP00000493146.1:n.715-86_715-85insGT
ENST00000641691.1:c.*480-86_*480-85insGT	ENSP00000492910.1:n.*480-86_*480-85insGT
ENST00000641924.1:c.*57-86_*57-85insGT	ENSP00000493063.1:n.*57-86_*57-85insGT
ENST00000642050.2:c.628-86_628-85insGT MANE Select	ENSP00000493153.1:n.628-86_628-85insGT
ENST00000372775.2:n.24+68_24+69insGT
ENST00000372779.8:c.715-86_715-85insGT	ENSP00000361865.4:n.715-86_715-85insGT
ENST00000433473.7:c.628-86_628-85insGT	ENSP00000394863.3:n.628-86_628-85insGT
ENST00000439754.5:c.313-86_313-85insGT	ENSP00000403207.1:n.313-86_313-85insGT
ENST00000449045.6:c.319-86_319-85insGT	ENSP00000392293.2:n.319-86_319-85insGT
ENST00000527311.6:c.403-86_403-85insGT	ENSP00000436695.2:n.403-86_403-85insGT
ENST00000529905.5:c.628-86_628-85insGT	ENSP00000432053.1:n.628-86_628-85insGT
ENST00000530076.5:c.-30-86_-30-85insGT	ENSP00000434007.1:n.-30-86_-30-85insGT
ENST00000530704.5:c.*251-86_*251-85insGT	ENSP00000431655.1:n.*251-86_*251-85insGT
NM_000310.3:c.628-86_628-85insGT , LRG_690t1:c.628-86_628-85insGT	NP_000301.1:n.628-86_628-85insGT
NM_001142604.1:c.319-86_319-85insGT	NP_001136076.1:n.319-86_319-85insGT
XM_005271008.1:c.628-86_628-85insGT	XP_005271065.1:n.628-86_628-85insGT
NM_001363695.1:c.628-86_628-85insGT	NP_001350624.1:n.628-86_628-85insGT
NM_000310.4:c.628-86_628-85insGT MANE Select	NP_000301.1:n.628-86_628-85insGT
NM_001142604.2:c.319-86_319-85insGT	NP_001136076.1:n.319-86_319-85insGT
NM_001363695.2:c.628-86_628-85insGT	NP_001350624.1:n.628-86_628-85insGT