Canonical Allele Identifier: CA339845662

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40539818T>C (hg19) ; chr1:g.40074146T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074146T>C , CM000663.2:g.40074146T>C	GRCh38
NC_000001.10:g.40539818T>C , CM000663.1:g.40539818T>C	GRCh37
NC_000001.9:g.40312405T>C	NCBI36
NG_009192.1:g.28325A>G , LRG_690:g.28325A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.833A>G	ENSP00000394863.4:p.Gln278Arg
ENST00000439754.6:c.764A>G	ENSP00000403207.2:p.Gln255Arg
ENST00000449045.7:c.527A>G	ENSP00000392293.2:p.Gln176Arg
ENST00000527311.7:c.605A>G	ENSP00000436695.3:p.Gln202Arg
ENST00000530076.6:c.179A>G	ENSP00000434007.1:p.Gln60Arg
ENST00000530704.6:c.*459A>G	ENSP00000431655.1:n.*459A>G
ENST00000641083.1:c.926A>G
ENST00000641236.1:n.1073A>G
ENST00000641319.1:c.*46A>G	ENSP00000493128.1:n.*46A>G
ENST00000641381.1:c.258A>G
ENST00000641471.1:c.923A>G	ENSP00000493146.1:p.Gln308Arg
ENST00000641691.1:c.*688A>G	ENSP00000492910.1:n.*688A>G
ENST00000641924.1:c.*265A>G	ENSP00000493063.1:n.*265A>G
ENST00000642050.2:c.836A>G MANE Select	ENSP00000493153.1:p.Gln279Arg
ENST00000372775.2:n.233A>G
ENST00000433473.7:c.836A>G	ENSP00000394863.3:p.Gln279Arg
ENST00000439754.5:c.449A>G	ENSP00000403207.1:p.Gln150Arg
ENST00000449045.6:c.527A>G	ENSP00000392293.2:p.Gln176Arg
ENST00000527311.6:c.611A>G	ENSP00000436695.2:p.Gln204Arg
ENST00000529905.5:c.836A>G	ENSP00000432053.1:p.Gln279Arg
ENST00000530076.5:c.179A>G	ENSP00000434007.1:p.Gln60Arg
ENST00000530704.5:c.*459A>G	ENSP00000431655.1:n.*459A>G
NM_000310.3:c.836A>G , LRG_690t1:c.836A>G	NP_000301.1:p.Gln279Arg
NM_001142604.1:c.527A>G	NP_001136076.1:p.Gln176Arg
XM_005271008.1:c.764A>G	XP_005271065.1:p.Gln255Arg
NM_001363695.1:c.764A>G	NP_001350624.1:p.Gln255Arg
NM_000310.4:c.836A>G MANE Select	NP_000301.1:p.Gln279Arg
NM_001142604.2:c.527A>G	NP_001136076.1:p.Gln176Arg
NM_001363695.2:c.764A>G	NP_001350624.1:p.Gln255Arg