Canonical Allele Identifier: CA339845411

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40539764A>G (hg19) ; chr1:g.40074092A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074092A>G , CM000663.2:g.40074092A>G	GRCh38
NC_000001.10:g.40539764A>G , CM000663.1:g.40539764A>G	GRCh37
NC_000001.9:g.40312351A>G	NCBI36
NG_009192.1:g.28379T>C , LRG_690:g.28379T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.887T>C	ENSP00000394863.4:p.Phe296Ser
ENST00000439754.6:c.818T>C	ENSP00000403207.2:p.Phe273Ser
ENST00000449045.7:c.581T>C	ENSP00000392293.2:p.Phe194Ser
ENST00000530076.6:c.233T>C	ENSP00000434007.1:p.Phe78Ser
ENST00000530704.6:c.*513T>C	ENSP00000431655.1:n.*513T>C
ENST00000641083.1:c.980T>C
ENST00000641236.1:n.1127T>C
ENST00000641319.1:c.*100T>C	ENSP00000493128.1:n.*100T>C
ENST00000641381.1:c.312T>C
ENST00000641471.1:c.977T>C	ENSP00000493146.1:p.Phe326Ser
ENST00000641691.1:c.*742T>C	ENSP00000492910.1:n.*742T>C
ENST00000641924.1:c.*319T>C	ENSP00000493063.1:n.*319T>C
ENST00000642050.2:c.890T>C MANE Select	ENSP00000493153.1:p.Phe297Ser
ENST00000372775.2:n.287T>C
ENST00000433473.7:c.890T>C	ENSP00000394863.3:p.Phe297Ser
ENST00000439754.5:c.503T>C	ENSP00000403207.1:p.Phe168Ser
ENST00000449045.6:c.581T>C	ENSP00000392293.2:p.Phe194Ser
ENST00000529905.5:c.890T>C	ENSP00000432053.1:p.Phe297Ser
ENST00000530076.5:c.233T>C	ENSP00000434007.1:p.Phe78Ser
ENST00000530704.5:c.*513T>C	ENSP00000431655.1:n.*513T>C
NM_000310.3:c.890T>C , LRG_690t1:c.890T>C	NP_000301.1:p.Phe297Ser
NM_001142604.1:c.581T>C	NP_001136076.1:p.Phe194Ser
XM_005271008.1:c.818T>C	XP_005271065.1:p.Phe273Ser
NM_001363695.1:c.818T>C	NP_001350624.1:p.Phe273Ser
NM_000310.4:c.890T>C MANE Select	NP_000301.1:p.Phe297Ser
NM_001142604.2:c.581T>C	NP_001136076.1:p.Phe194Ser
NM_001363695.2:c.818T>C	NP_001350624.1:p.Phe273Ser