Canonical Allele Identifier: CA417322850

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40558078G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092406G>A , CM000663.2:g.40092406G>A	GRCh38
NC_000001.10:g.40558078G>A , CM000663.1:g.40558078G>A	GRCh37
NC_000001.9:g.40330665G>A	NCBI36
NG_009192.1:g.10065C>T , LRG_690:g.10065C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*62C>T	ENSP00000361865.5:n.*62C>T
ENST00000433473.8:c.223C>T	ENSP00000394863.4:p.Leu75=
ENST00000439754.6:c.226C>T	ENSP00000403207.2:p.Leu76=
ENST00000449045.7:c.125-2894C>T	ENSP00000392293.2:n.125-2894C>T
ENST00000526547.2:c.506C>T
ENST00000527311.7:c.226C>T	ENSP00000436695.3:p.Leu76=
ENST00000530704.6:c.226C>T	ENSP00000431655.1:p.Leu76=
ENST00000641083.1:c.204C>T
ENST00000641236.1:n.238C>T
ENST00000641319.1:c.226C>T	ENSP00000493128.1:p.Leu76=
ENST00000641471.1:c.313C>T	ENSP00000493146.1:p.Leu105=
ENST00000641548.1:c.*78C>T	ENSP00000492984.1:n.*78C>T
ENST00000641691.1:c.*78C>T	ENSP00000492910.1:n.*78C>T
ENST00000641924.1:c.124+4709C>T	ENSP00000493063.1:n.124+4709C>T
ENST00000642050.2:c.226C>T MANE Select	ENSP00000493153.1:p.Leu76=
ENST00000372779.8:c.313C>T	ENSP00000361865.4:p.Leu105=
ENST00000433473.7:c.226C>T	ENSP00000394863.3:p.Leu76=
ENST00000449045.6:c.125-2894C>T	ENSP00000392293.2:n.125-2894C>T
ENST00000526547.1:c.76C>T	ENSP00000436481.1:p.Leu26=
ENST00000527311.6:c.125-349C>T	ENSP00000436695.2:n.125-349C>T
ENST00000529905.5:c.226C>T	ENSP00000432053.1:p.Leu76=
ENST00000530704.5:c.226C>T	ENSP00000431655.1:p.Leu76=
NM_000310.3:c.226C>T , LRG_690t1:c.226C>T	NP_000301.1:p.Leu76=
NM_001142604.1:c.125-2894C>T	NP_001136076.1:n.125-2894C>T
XM_005271008.1:c.226C>T	XP_005271065.1:p.Leu76=
NM_001363695.1:c.226C>T	NP_001350624.1:p.Leu76=
NM_000310.4:c.226C>T MANE Select	NP_000301.1:p.Leu76=
NM_001142604.2:c.125-2894C>T	NP_001136076.1:n.125-2894C>T
NM_001363695.2:c.226C>T	NP_001350624.1:p.Leu76=