Canonical Allele Identifier: CA2743276765

Gene: PPT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091500_40091501insGT , CM000663.2:g.40091500_40091501insGT	GRCh38
NC_000001.10:g.40557172_40557173insGT , CM000663.1:g.40557172_40557173insGT	GRCh37
NC_000001.9:g.40329759_40329760insGT	NCBI36
NG_009192.1:g.10970_10971insAC , LRG_690:g.10970_10971insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*199-102_*199-101insAC	ENSP00000361865.5:n.*199-102_*199-101insAC
ENST00000433473.8:c.360-102_360-101insAC	ENSP00000394863.4:n.360-102_360-101insAC
ENST00000439754.6:c.363-102_363-101insAC	ENSP00000403207.2:n.363-102_363-101insAC
ENST00000449045.7:c.125-1989_125-1988insAC	ENSP00000392293.2:n.125-1989_125-1988insAC
ENST00000526547.2:c.643-102_643-101insAC
ENST00000527311.7:c.235-102_235-101insAC	ENSP00000436695.3:n.235-102_235-101insAC
ENST00000530704.6:c.363-102_363-101insAC	ENSP00000431655.1:n.363-102_363-101insAC
ENST00000641083.1:c.341-102_341-101insAC
ENST00000641236.1:n.600-102_600-101insAC
ENST00000641319.1:c.363-102_363-101insAC	ENSP00000493128.1:n.363-102_363-101insAC
ENST00000641471.1:c.450-102_450-101insAC	ENSP00000493146.1:n.450-102_450-101insAC
ENST00000641548.1:c.*215-102_*215-101insAC	ENSP00000492984.1:n.*215-102_*215-101insAC
ENST00000641691.1:c.*215-102_*215-101insAC	ENSP00000492910.1:n.*215-102_*215-101insAC
ENST00000641924.1:c.124+5614_124+5615insAC	ENSP00000493063.1:n.124+5614_124+5615insAC
ENST00000642050.2:c.363-102_363-101insAC MANE Select	ENSP00000493153.1:n.363-102_363-101insAC
ENST00000372779.8:c.450-102_450-101insAC	ENSP00000361865.4:n.450-102_450-101insAC
ENST00000433473.7:c.363-102_363-101insAC	ENSP00000394863.3:n.363-102_363-101insAC
ENST00000439754.5:c.48-102_48-101insAC	ENSP00000403207.1:n.48-102_48-101insAC
ENST00000449045.6:c.125-1989_125-1988insAC	ENSP00000392293.2:n.125-1989_125-1988insAC
ENST00000526547.1:c.213-102_213-101insAC	ENSP00000436481.1:n.213-102_213-101insAC
ENST00000527311.6:c.138-102_138-101insAC	ENSP00000436695.2:n.138-102_138-101insAC
ENST00000529905.5:c.363-102_363-101insAC	ENSP00000432053.1:n.363-102_363-101insAC
ENST00000530704.5:c.363-102_363-101insAC	ENSP00000431655.1:n.363-102_363-101insAC
NM_000310.3:c.363-102_363-101insAC , LRG_690t1:c.363-102_363-101insAC	NP_000301.1:n.363-102_363-101insAC
NM_001142604.1:c.125-1989_125-1988insAC	NP_001136076.1:n.125-1989_125-1988insAC
XM_005271008.1:c.363-102_363-101insAC	XP_005271065.1:n.363-102_363-101insAC
NM_001363695.1:c.363-102_363-101insAC	NP_001350624.1:n.363-102_363-101insAC
NM_000310.4:c.363-102_363-101insAC MANE Select	NP_000301.1:n.363-102_363-101insAC
NM_001142604.2:c.125-1989_125-1988insAC	NP_001136076.1:n.125-1989_125-1988insAC
NM_001363695.2:c.363-102_363-101insAC	NP_001350624.1:n.363-102_363-101insAC