Canonical Allele Identifier: CA417322716

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557023G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40091351G>T , CM000663.2:g.40091351G>T	GRCh38
NC_000001.10:g.40557023G>T , CM000663.1:g.40557023G>T	GRCh37
NC_000001.9:g.40329610G>T	NCBI36
NG_009192.1:g.11120C>A , LRG_690:g.11120C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000372779.9:c.*247C>A	ENSP00000361865.5:n.*247C>A
ENST00000433473.8:c.408C>A	ENSP00000394863.4:p.Ile136=
ENST00000439754.6:c.411C>A	ENSP00000403207.2:p.Ile137=
ENST00000449045.7:c.125-1839C>A	ENSP00000392293.2:n.125-1839C>A
ENST00000526547.2:c.691C>A
ENST00000527311.7:c.283C>A	ENSP00000436695.3:p.Leu95Ile
ENST00000530704.6:c.411C>A	ENSP00000431655.1:p.Ile137=
ENST00000641083.1:c.389C>A
ENST00000641236.1:n.648C>A
ENST00000641319.1:c.411C>A	ENSP00000493128.1:p.Ile137=
ENST00000641381.1:c.23C>A
ENST00000641471.1:c.498C>A	ENSP00000493146.1:p.Ile166=
ENST00000641548.1:c.*263C>A	ENSP00000492984.1:n.*263C>A
ENST00000641691.1:c.*263C>A	ENSP00000492910.1:n.*263C>A
ENST00000641924.1:c.124+5764C>A	ENSP00000493063.1:n.124+5764C>A
ENST00000642050.2:c.411C>A MANE Select	ENSP00000493153.1:p.Ile137=
ENST00000372779.8:c.498C>A	ENSP00000361865.4:p.Ile166=
ENST00000433473.7:c.411C>A	ENSP00000394863.3:p.Ile137=
ENST00000439754.5:c.96C>A	ENSP00000403207.1:p.Ile32=
ENST00000449045.6:c.125-1839C>A	ENSP00000392293.2:n.125-1839C>A
ENST00000526547.1:c.261C>A	ENSP00000436481.1:p.Ile87=
ENST00000527311.6:c.186C>A	ENSP00000436695.2:p.Ile62=
ENST00000529905.5:c.411C>A	ENSP00000432053.1:p.Ile137=
ENST00000530704.5:c.411C>A	ENSP00000431655.1:p.Ile137=
NM_000310.3:c.411C>A , LRG_690t1:c.411C>A	NP_000301.1:p.Ile137=
NM_001142604.1:c.125-1839C>A	NP_001136076.1:n.125-1839C>A
XM_005271008.1:c.411C>A	XP_005271065.1:p.Ile137=
NM_001363695.1:c.411C>A	NP_001350624.1:p.Ile137=
NM_000310.4:c.411C>A MANE Select	NP_000301.1:p.Ile137=
NM_001142604.2:c.125-1839C>A	NP_001136076.1:n.125-1839C>A
NM_001363695.2:c.411C>A	NP_001350624.1:p.Ile137=