Canonical Allele Identifier: CA339845650

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40539815A>T (hg19) ; chr1:g.40074143A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074143A>T , CM000663.2:g.40074143A>T	GRCh38
NC_000001.10:g.40539815A>T , CM000663.1:g.40539815A>T	GRCh37
NC_000001.9:g.40312402A>T	NCBI36
NG_009192.1:g.28328T>A , LRG_690:g.28328T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.836T>A	ENSP00000394863.4:p.Leu279Gln
ENST00000439754.6:c.767T>A	ENSP00000403207.2:p.Leu256Gln
ENST00000449045.7:c.530T>A	ENSP00000392293.2:p.Leu177Gln
ENST00000527311.7:c.608T>A	ENSP00000436695.3:p.Leu203Gln
ENST00000530076.6:c.182T>A	ENSP00000434007.1:p.Leu61Gln
ENST00000530704.6:c.*462T>A	ENSP00000431655.1:n.*462T>A
ENST00000641083.1:c.929T>A
ENST00000641236.1:n.1076T>A
ENST00000641319.1:c.*49T>A	ENSP00000493128.1:n.*49T>A
ENST00000641381.1:c.261T>A
ENST00000641471.1:c.926T>A	ENSP00000493146.1:p.Leu309Gln
ENST00000641691.1:c.*691T>A	ENSP00000492910.1:n.*691T>A
ENST00000641924.1:c.*268T>A	ENSP00000493063.1:n.*268T>A
ENST00000642050.2:c.839T>A MANE Select	ENSP00000493153.1:p.Leu280Gln
ENST00000372775.2:n.236T>A
ENST00000433473.7:c.839T>A	ENSP00000394863.3:p.Leu280Gln
ENST00000439754.5:c.452T>A	ENSP00000403207.1:p.Leu151Gln
ENST00000449045.6:c.530T>A	ENSP00000392293.2:p.Leu177Gln
ENST00000527311.6:c.614T>A
ENST00000529905.5:c.839T>A	ENSP00000432053.1:p.Leu280Gln
ENST00000530076.5:c.182T>A	ENSP00000434007.1:p.Leu61Gln
ENST00000530704.5:c.*462T>A	ENSP00000431655.1:n.*462T>A
NM_000310.3:c.839T>A , LRG_690t1:c.839T>A	NP_000301.1:p.Leu280Gln
NM_001142604.1:c.530T>A	NP_001136076.1:p.Leu177Gln
XM_005271008.1:c.767T>A	XP_005271065.1:p.Leu256Gln
NM_001363695.1:c.767T>A	NP_001350624.1:p.Leu256Gln
NM_000310.4:c.839T>A MANE Select	NP_000301.1:p.Leu280Gln
NM_001142604.2:c.530T>A	NP_001136076.1:p.Leu177Gln
NM_001363695.2:c.767T>A	NP_001350624.1:p.Leu256Gln