Canonical Allele Identifier: CA339846572

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40544239T>A (hg19) ; chr1:g.40078567T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40078567T>A , CM000663.2:g.40078567T>A	GRCh38
NC_000001.10:g.40544239T>A , CM000663.1:g.40544239T>A	GRCh37
NC_000001.9:g.40316826T>A	NCBI36
NG_009192.1:g.23904A>T , LRG_690:g.23904A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.716A>T	ENSP00000394863.4:p.Asp239Val
ENST00000439754.6:c.719A>T	ENSP00000403207.2:p.Asp240Val
ENST00000449045.7:c.410A>T	ENSP00000392293.2:p.Asp137Val
ENST00000527311.7:c.488A>T	ENSP00000436695.3:p.Asp163Val
ENST00000530076.6:c.62A>T	ENSP00000434007.1:p.Asp21Val
ENST00000530704.6:c.*342A>T	ENSP00000431655.1:n.*342A>T
ENST00000641083.1:c.697A>T
ENST00000641236.1:n.956A>T
ENST00000641319.1:c.719A>T	ENSP00000493128.1:p.Asp240Val
ENST00000641381.1:c.149-1654A>T
ENST00000641471.1:c.806A>T	ENSP00000493146.1:p.Asp269Val
ENST00000641691.1:c.*571A>T	ENSP00000492910.1:n.*571A>T
ENST00000641924.1:c.*148A>T	ENSP00000493063.1:n.*148A>T
ENST00000642050.2:c.719A>T MANE Select	ENSP00000493153.1:p.Asp240Val
ENST00000372775.2:n.116A>T
ENST00000372779.8:c.806A>T	ENSP00000361865.4:p.Asp269Val
ENST00000433473.7:c.719A>T	ENSP00000394863.3:p.Asp240Val
ENST00000439754.5:c.404A>T	ENSP00000403207.1:p.Asp135Val
ENST00000449045.6:c.410A>T	ENSP00000392293.2:p.Asp137Val
ENST00000527311.6:c.494A>T	ENSP00000436695.2:p.Asp165Val
ENST00000529905.5:c.719A>T	ENSP00000432053.1:p.Asp240Val
ENST00000530076.5:c.62A>T	ENSP00000434007.1:p.Asp21Val
ENST00000530704.5:c.*342A>T	ENSP00000431655.1:n.*342A>T
NM_000310.3:c.719A>T , LRG_690t1:c.719A>T	NP_000301.1:p.Asp240Val
NM_001142604.1:c.410A>T	NP_001136076.1:p.Asp137Val
XM_005271008.1:c.719A>T	XP_005271065.1:p.Asp240Val
NM_001363695.1:c.719A>T	NP_001350624.1:p.Asp240Val
NM_000310.4:c.719A>T MANE Select	NP_000301.1:p.Asp240Val
NM_001142604.2:c.410A>T	NP_001136076.1:p.Asp137Val
NM_001363695.2:c.719A>T	NP_001350624.1:p.Asp240Val