Canonical Allele Identifier: CA339845536

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40539789G>A (hg19) ; chr1:g.40074117G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40074117G>A , CM000663.2:g.40074117G>A	GRCh38
NC_000001.10:g.40539789G>A , CM000663.1:g.40539789G>A	GRCh37
NC_000001.9:g.40312376G>A	NCBI36
NG_009192.1:g.28354C>T , LRG_690:g.28354C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.862C>T	ENSP00000394863.4:p.His288Tyr
ENST00000439754.6:c.793C>T	ENSP00000403207.2:p.His265Tyr
ENST00000449045.7:c.556C>T	ENSP00000392293.2:p.His186Tyr
ENST00000530076.6:c.208C>T	ENSP00000434007.1:p.His70Tyr
ENST00000530704.6:c.*488C>T	ENSP00000431655.1:n.*488C>T
ENST00000641083.1:c.955C>T
ENST00000641236.1:n.1102C>T
ENST00000641319.1:c.*75C>T	ENSP00000493128.1:n.*75C>T
ENST00000641381.1:c.287C>T
ENST00000641471.1:c.952C>T	ENSP00000493146.1:p.His318Tyr
ENST00000641691.1:c.*717C>T	ENSP00000492910.1:n.*717C>T
ENST00000641924.1:c.*294C>T	ENSP00000493063.1:n.*294C>T
ENST00000642050.2:c.865C>T MANE Select	ENSP00000493153.1:p.His289Tyr
ENST00000372775.2:n.262C>T
ENST00000433473.7:c.865C>T	ENSP00000394863.3:p.His289Tyr
ENST00000439754.5:c.478C>T	ENSP00000403207.1:p.His160Tyr
ENST00000449045.6:c.556C>T	ENSP00000392293.2:p.His186Tyr
ENST00000529905.5:c.865C>T	ENSP00000432053.1:p.His289Tyr
ENST00000530076.5:c.208C>T	ENSP00000434007.1:p.His70Tyr
ENST00000530704.5:c.*488C>T	ENSP00000431655.1:n.*488C>T
NM_000310.3:c.865C>T , LRG_690t1:c.865C>T	NP_000301.1:p.His289Tyr
NM_001142604.1:c.556C>T	NP_001136076.1:p.His186Tyr
XM_005271008.1:c.793C>T	XP_005271065.1:p.His265Tyr
NM_001363695.1:c.793C>T	NP_001350624.1:p.His265Tyr
NM_000310.4:c.865C>T MANE Select	NP_000301.1:p.His289Tyr
NM_001142604.2:c.556C>T	NP_001136076.1:p.His186Tyr
NM_001363695.2:c.793C>T	NP_001350624.1:p.His265Tyr