Canonical Allele Identifier: CA2743276932

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40078781_40078782insA , CM000663.2:g.40078781_40078782insA	GRCh38
NC_000001.10:g.40544453_40544454insA , CM000663.1:g.40544453_40544454insA	GRCh37
NC_000001.9:g.40317040_40317041insA	NCBI36
NG_009192.1:g.23689_23690insT , LRG_690:g.23689_23690insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.625-124_625-123insT	ENSP00000394863.4:n.625-124_625-123insT
ENST00000439754.6:c.628-124_628-123insT	ENSP00000403207.2:n.628-124_628-123insT
ENST00000449045.7:c.319-124_319-123insT	ENSP00000392293.2:n.319-124_319-123insT
ENST00000527311.7:c.397-124_397-123insT	ENSP00000436695.3:n.397-124_397-123insT
ENST00000530076.6:c.-30-124_-30-123insT	ENSP00000434007.1:n.-30-124_-30-123insT
ENST00000530704.6:c.*251-124_*251-123insT	ENSP00000431655.1:n.*251-124_*251-123insT
ENST00000641083.1:c.606-124_606-123insT
ENST00000641236.1:n.865-124_865-123insT
ENST00000641319.1:c.628-124_628-123insT	ENSP00000493128.1:n.628-124_628-123insT
ENST00000641381.1:c.149-1869_149-1868insT
ENST00000641471.1:c.715-124_715-123insT	ENSP00000493146.1:n.715-124_715-123insT
ENST00000641691.1:c.*480-124_*480-123insT	ENSP00000492910.1:n.*480-124_*480-123insT
ENST00000641924.1:c.*57-124_*57-123insT	ENSP00000493063.1:n.*57-124_*57-123insT
ENST00000642050.2:c.628-124_628-123insT MANE Select	ENSP00000493153.1:n.628-124_628-123insT
ENST00000372775.2:n.24+30_24+31insT
ENST00000372779.8:c.715-124_715-123insT	ENSP00000361865.4:n.715-124_715-123insT
ENST00000433473.7:c.628-124_628-123insT	ENSP00000394863.3:n.628-124_628-123insT
ENST00000439754.5:c.313-124_313-123insT	ENSP00000403207.1:n.313-124_313-123insT
ENST00000449045.6:c.319-124_319-123insT	ENSP00000392293.2:n.319-124_319-123insT
ENST00000527311.6:c.403-124_403-123insT	ENSP00000436695.2:n.403-124_403-123insT
ENST00000529905.5:c.628-124_628-123insT	ENSP00000432053.1:n.628-124_628-123insT
ENST00000530076.5:c.-30-124_-30-123insT	ENSP00000434007.1:n.-30-124_-30-123insT
ENST00000530704.5:c.*251-124_*251-123insT	ENSP00000431655.1:n.*251-124_*251-123insT
NM_000310.3:c.628-124_628-123insT , LRG_690t1:c.628-124_628-123insT	NP_000301.1:n.628-124_628-123insT
NM_001142604.1:c.319-124_319-123insT	NP_001136076.1:n.319-124_319-123insT
XM_005271008.1:c.628-124_628-123insT	XP_005271065.1:n.628-124_628-123insT
NM_001363695.1:c.628-124_628-123insT	NP_001350624.1:n.628-124_628-123insT
NM_000310.4:c.628-124_628-123insT MANE Select	NP_000301.1:n.628-124_628-123insT
NM_001142604.2:c.319-124_319-123insT	NP_001136076.1:n.319-124_319-123insT
NM_001363695.2:c.628-124_628-123insT	NP_001350624.1:n.628-124_628-123insT