Canonical Allele Identifier: CA339847619

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40546088G>A (hg19) ; chr1:g.40080416G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40080416G>A , CM000663.2:g.40080416G>A	GRCh38
NC_000001.10:g.40546088G>A , CM000663.1:g.40546088G>A	GRCh37
NC_000001.9:g.40318675G>A	NCBI36
NG_009192.1:g.22055C>T , LRG_690:g.22055C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433473.8:c.605C>T	ENSP00000394863.4:p.Ala202Val
ENST00000439754.6:c.608C>T	ENSP00000403207.2:p.Ala203Val
ENST00000449045.7:c.299C>T	ENSP00000392293.2:p.Ala100Val
ENST00000527311.7:c.377C>T	ENSP00000436695.3:p.Ala126Val
ENST00000530076.6:c.-50C>T	ENSP00000434007.1:n.-50C>T
ENST00000530704.6:c.*231C>T	ENSP00000431655.1:n.*231C>T
ENST00000641083.1:c.586C>T
ENST00000641236.1:n.845C>T
ENST00000641319.1:c.608C>T	ENSP00000493128.1:p.Ala203Val
ENST00000641381.1:c.149-3503C>T
ENST00000641471.1:c.695C>T	ENSP00000493146.1:p.Ala232Val
ENST00000641691.1:c.*460C>T	ENSP00000492910.1:n.*460C>T
ENST00000641924.1:c.*37C>T	ENSP00000493063.1:n.*37C>T
ENST00000642050.2:c.608C>T MANE Select	ENSP00000493153.1:p.Ala203Val
ENST00000372779.8:c.695C>T	ENSP00000361865.4:p.Ala232Val
ENST00000433473.7:c.608C>T	ENSP00000394863.3:p.Ala203Val
ENST00000439754.5:c.293C>T	ENSP00000403207.1:p.Ala98Val
ENST00000449045.6:c.299C>T	ENSP00000392293.2:p.Ala100Val
ENST00000527311.6:c.383C>T	ENSP00000436695.2:p.Ala128Val
ENST00000529905.5:c.608C>T	ENSP00000432053.1:p.Ala203Val
ENST00000530076.5:c.-50C>T	ENSP00000434007.1:n.-50C>T
ENST00000530704.5:c.*231C>T	ENSP00000431655.1:n.*231C>T
NM_000310.3:c.608C>T , LRG_690t1:c.608C>T	NP_000301.1:p.Ala203Val
NM_001142604.1:c.299C>T	NP_001136076.1:p.Ala100Val
XM_005271008.1:c.608C>T	XP_005271065.1:p.Ala203Val
NM_001363695.1:c.608C>T	NP_001350624.1:p.Ala203Val
NM_000310.4:c.608C>T MANE Select	NP_000301.1:p.Ala203Val
NM_001142604.2:c.299C>T	NP_001136076.1:p.Ala100Val
NM_001363695.2:c.608C>T	NP_001350624.1:p.Ala203Val