Canonical Allele Identifier: CA339845538

Gene: PPT1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.862C>G	ENSP00000394863.4:p.His288Asp
ENST00000439754.6:c.793C>G	ENSP00000403207.2:p.His265Asp
ENST00000449045.7:c.556C>G	ENSP00000392293.2:p.His186Asp
ENST00000530076.6:c.208C>G	ENSP00000434007.1:p.His70Asp
ENST00000530704.6:c.*488C>G	ENSP00000431655.1:n.*488C>G
ENST00000641083.1:c.955C>G
ENST00000641236.1:n.1102C>G
ENST00000641319.1:c.*75C>G	ENSP00000493128.1:n.*75C>G
ENST00000641381.1:c.287C>G
ENST00000641471.1:c.952C>G	ENSP00000493146.1:p.His318Asp
ENST00000641691.1:c.*717C>G	ENSP00000492910.1:n.*717C>G
ENST00000641924.1:c.*294C>G	ENSP00000493063.1:n.*294C>G
ENST00000642050.2:c.865C>G MANE Select	ENSP00000493153.1:p.His289Asp
ENST00000372775.2:n.262C>G
ENST00000433473.7:c.865C>G	ENSP00000394863.3:p.His289Asp
ENST00000439754.5:c.478C>G	ENSP00000403207.1:p.His160Asp
ENST00000449045.6:c.556C>G	ENSP00000392293.2:p.His186Asp
ENST00000529905.5:c.865C>G	ENSP00000432053.1:p.His289Asp
ENST00000530076.5:c.208C>G	ENSP00000434007.1:p.His70Asp
ENST00000530704.5:c.*488C>G	ENSP00000431655.1:n.*488C>G
NM_000310.3:c.865C>G , LRG_690t1:c.865C>G	NP_000301.1:p.His289Asp
NM_001142604.1:c.556C>G	NP_001136076.1:p.His186Asp
XM_005271008.1:c.793C>G	XP_005271065.1:p.His265Asp
NM_001363695.1:c.793C>G	NP_001350624.1:p.His265Asp
NM_000310.4:c.865C>G MANE Select	NP_000301.1:p.His289Asp
NM_001142604.2:c.556C>G	NP_001136076.1:p.His186Asp
NM_001363695.2:c.793C>G	NP_001350624.1:p.His265Asp