Canonical Allele Identifier: CA339846645

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40544257G>A (hg19) ; chr1:g.40078585G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40078585G>A , CM000663.2:g.40078585G>A	GRCh38
NC_000001.10:g.40544257G>A , CM000663.1:g.40544257G>A	GRCh37
NC_000001.9:g.40316844G>A	NCBI36
NG_009192.1:g.23886C>T , LRG_690:g.23886C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.698C>T	ENSP00000394863.4:p.Ser233Phe
ENST00000439754.6:c.701C>T	ENSP00000403207.2:p.Ser234Phe
ENST00000449045.7:c.392C>T	ENSP00000392293.2:p.Ser131Phe
ENST00000527311.7:c.470C>T	ENSP00000436695.3:p.Ser157Phe
ENST00000530076.6:c.44C>T	ENSP00000434007.1:p.Ser15Phe
ENST00000530704.6:c.*324C>T	ENSP00000431655.1:n.*324C>T
ENST00000641083.1:c.679C>T
ENST00000641236.1:n.938C>T
ENST00000641319.1:c.701C>T	ENSP00000493128.1:p.Ser234Phe
ENST00000641381.1:c.149-1672C>T
ENST00000641471.1:c.788C>T	ENSP00000493146.1:p.Ser263Phe
ENST00000641691.1:c.*553C>T	ENSP00000492910.1:n.*553C>T
ENST00000641924.1:c.*130C>T	ENSP00000493063.1:n.*130C>T
ENST00000642050.2:c.701C>T MANE Select	ENSP00000493153.1:p.Ser234Phe
ENST00000372775.2:n.98C>T
ENST00000372779.8:c.788C>T	ENSP00000361865.4:p.Ser263Phe
ENST00000433473.7:c.701C>T	ENSP00000394863.3:p.Ser234Phe
ENST00000439754.5:c.386C>T	ENSP00000403207.1:p.Ser129Phe
ENST00000449045.6:c.392C>T	ENSP00000392293.2:p.Ser131Phe
ENST00000527311.6:c.476C>T	ENSP00000436695.2:p.Ser159Phe
ENST00000529905.5:c.701C>T	ENSP00000432053.1:p.Ser234Phe
ENST00000530076.5:c.44C>T	ENSP00000434007.1:p.Ser15Phe
ENST00000530704.5:c.*324C>T	ENSP00000431655.1:n.*324C>T
NM_000310.3:c.701C>T , LRG_690t1:c.701C>T	NP_000301.1:p.Ser234Phe
NM_001142604.1:c.392C>T	NP_001136076.1:p.Ser131Phe
XM_005271008.1:c.701C>T	XP_005271065.1:p.Ser234Phe
NM_001363695.1:c.701C>T	NP_001350624.1:p.Ser234Phe
NM_000310.4:c.701C>T MANE Select	NP_000301.1:p.Ser234Phe
NM_001142604.2:c.392C>T	NP_001136076.1:p.Ser131Phe
NM_001363695.2:c.701C>T	NP_001350624.1:p.Ser234Phe