Canonical Allele Identifier: CA417322762

Gene: PPT1

Linked Data

• MyVariant Identifiers: chr1:g.40557728T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092056T>A , CM000663.2:g.40092056T>A	GRCh38
NC_000001.10:g.40557728T>A , CM000663.1:g.40557728T>A	GRCh37
NC_000001.9:g.40330315T>A	NCBI36
NG_009192.1:g.10415A>T , LRG_690:g.10415A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*187A>T	ENSP00000361865.5:n.*187A>T
ENST00000433473.8:c.348A>T	ENSP00000394863.4:p.Gly116=
ENST00000439754.6:c.351A>T	ENSP00000403207.2:p.Gly117=
ENST00000449045.7:c.125-2544A>T	ENSP00000392293.2:n.125-2544A>T
ENST00000526547.2:c.631A>T
ENST00000527311.7:c.234+342A>T	ENSP00000436695.3:n.234+342A>T
ENST00000530704.6:c.351A>T	ENSP00000431655.1:p.Gly117=
ENST00000641083.1:c.329A>T
ENST00000641236.1:n.588A>T
ENST00000641319.1:c.351A>T	ENSP00000493128.1:p.Gly117=
ENST00000641471.1:c.438A>T	ENSP00000493146.1:p.Gly146=
ENST00000641548.1:c.*203A>T	ENSP00000492984.1:n.*203A>T
ENST00000641691.1:c.*203A>T	ENSP00000492910.1:n.*203A>T
ENST00000641924.1:c.124+5059A>T	ENSP00000493063.1:n.124+5059A>T
ENST00000642050.2:c.351A>T MANE Select	ENSP00000493153.1:p.Gly117=
ENST00000372779.8:c.438A>T	ENSP00000361865.4:p.Gly146=
ENST00000433473.7:c.351A>T	ENSP00000394863.3:p.Gly117=
ENST00000439754.5:c.36A>T	ENSP00000403207.1:p.Gly12=
ENST00000449045.6:c.125-2544A>T	ENSP00000392293.2:n.125-2544A>T
ENST00000526547.1:c.201A>T	ENSP00000436481.1:p.Gly67=
ENST00000527311.6:c.126A>T	ENSP00000436695.2:p.Gly42=
ENST00000529905.5:c.351A>T	ENSP00000432053.1:p.Gly117=
ENST00000530704.5:c.351A>T	ENSP00000431655.1:p.Gly117=
NM_000310.3:c.351A>T , LRG_690t1:c.351A>T	NP_000301.1:p.Gly117=
NM_001142604.1:c.125-2544A>T	NP_001136076.1:n.125-2544A>T
XM_005271008.1:c.351A>T	XP_005271065.1:p.Gly117=
NM_001363695.1:c.351A>T	NP_001350624.1:p.Gly117=
NM_000310.4:c.351A>T MANE Select	NP_000301.1:p.Gly117=
NM_001142604.2:c.125-2544A>T	NP_001136076.1:n.125-2544A>T
NM_001363695.2:c.351A>T	NP_001350624.1:p.Gly117=