Canonical Allele Identifier: CA339847670

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40546098T>G (hg19) ; chr1:g.40080426T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40080426T>G , CM000663.2:g.40080426T>G	GRCh38
NC_000001.10:g.40546098T>G , CM000663.1:g.40546098T>G	GRCh37
NC_000001.9:g.40318685T>G	NCBI36
NG_009192.1:g.22045A>C , LRG_690:g.22045A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.595A>C	ENSP00000394863.4:p.Ile199Leu
ENST00000439754.6:c.598A>C	ENSP00000403207.2:p.Ile200Leu
ENST00000449045.7:c.289A>C	ENSP00000392293.2:p.Ile97Leu
ENST00000527311.7:c.367A>C	ENSP00000436695.3:p.Ile123Leu
ENST00000530076.6:c.-60A>C	ENSP00000434007.1:n.-60A>C
ENST00000530704.6:c.*221A>C	ENSP00000431655.1:n.*221A>C
ENST00000641083.1:c.576A>C
ENST00000641236.1:n.835A>C
ENST00000641319.1:c.598A>C	ENSP00000493128.1:p.Ile200Leu
ENST00000641381.1:c.149-3513A>C
ENST00000641471.1:c.685A>C	ENSP00000493146.1:p.Ile229Leu
ENST00000641691.1:c.*450A>C	ENSP00000492910.1:n.*450A>C
ENST00000641924.1:c.*27A>C	ENSP00000493063.1:n.*27A>C
ENST00000642050.2:c.598A>C MANE Select	ENSP00000493153.1:p.Ile200Leu
ENST00000372779.8:c.685A>C	ENSP00000361865.4:p.Ile229Leu
ENST00000433473.7:c.598A>C	ENSP00000394863.3:p.Ile200Leu
ENST00000439754.5:c.283A>C	ENSP00000403207.1:p.Ile95Leu
ENST00000449045.6:c.289A>C	ENSP00000392293.2:p.Ile97Leu
ENST00000527311.6:c.373A>C	ENSP00000436695.2:p.Ile125Leu
ENST00000529905.5:c.598A>C	ENSP00000432053.1:p.Ile200Leu
ENST00000530076.5:c.-60A>C	ENSP00000434007.1:n.-60A>C
ENST00000530704.5:c.*221A>C	ENSP00000431655.1:n.*221A>C
NM_000310.3:c.598A>C , LRG_690t1:c.598A>C	NP_000301.1:p.Ile200Leu
NM_001142604.1:c.289A>C	NP_001136076.1:p.Ile97Leu
XM_005271008.1:c.598A>C	XP_005271065.1:p.Ile200Leu
NM_001363695.1:c.598A>C	NP_001350624.1:p.Ile200Leu
NM_000310.4:c.598A>C MANE Select	NP_000301.1:p.Ile200Leu
NM_001142604.2:c.289A>C	NP_001136076.1:p.Ile97Leu
NM_001363695.2:c.598A>C	NP_001350624.1:p.Ile200Leu