Canonical Allele Identifier: CA417322968

Gene: PPT1

Linked Data

• gnomAD v4: 1-40092488-G-C
• MyVariant Identifiers: chr1:g.40558160G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092488G>C , CM000663.2:g.40092488G>C	GRCh38
NC_000001.10:g.40558160G>C , CM000663.1:g.40558160G>C	GRCh37
NC_000001.9:g.40330747G>C	NCBI36
NG_009192.1:g.9983C>G , LRG_690:g.9983C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.148C>G	ENSP00000361865.5:p.Leu50Val
ENST00000433473.8:c.141C>G	ENSP00000394863.4:p.Pro47=
ENST00000439754.6:c.144C>G	ENSP00000403207.2:p.Pro48=
ENST00000449045.7:c.125-2976C>G	ENSP00000392293.2:n.125-2976C>G
ENST00000526547.2:c.424C>G
ENST00000527311.7:c.144C>G	ENSP00000436695.3:p.Pro48=
ENST00000530704.6:c.144C>G	ENSP00000431655.1:p.Pro48=
ENST00000641083.1:c.122C>G
ENST00000641236.1:n.156C>G
ENST00000641319.1:c.144C>G	ENSP00000493128.1:p.Pro48=
ENST00000641471.1:c.231C>G	ENSP00000493146.1:p.Pro77=
ENST00000641548.1:c.137C>G	ENSP00000492984.1:p.Pro46Arg
ENST00000641691.1:c.137C>G	ENSP00000492910.1:p.Pro46Arg
ENST00000641924.1:c.124+4627C>G	ENSP00000493063.1:n.124+4627C>G
ENST00000642050.2:c.144C>G MANE Select	ENSP00000493153.1:p.Pro48=
ENST00000372779.8:c.231C>G	ENSP00000361865.4:p.Pro77=
ENST00000433473.7:c.144C>G	ENSP00000394863.3:p.Pro48=
ENST00000449045.6:c.125-2976C>G	ENSP00000392293.2:n.125-2976C>G
ENST00000526547.1:c.-7C>G	ENSP00000436481.1:n.-7C>G
ENST00000527311.6:c.125-431C>G	ENSP00000436695.2:n.125-431C>G
ENST00000529905.5:c.144C>G	ENSP00000432053.1:p.Pro48=
ENST00000530704.5:c.144C>G	ENSP00000431655.1:p.Pro48=
NM_000310.3:c.144C>G , LRG_690t1:c.144C>G	NP_000301.1:p.Pro48=
NM_001142604.1:c.125-2976C>G	NP_001136076.1:n.125-2976C>G
XM_005271008.1:c.144C>G	XP_005271065.1:p.Pro48=
NM_001363695.1:c.144C>G	NP_001350624.1:p.Pro48=
NM_000310.4:c.144C>G MANE Select	NP_000301.1:p.Pro48=
NM_001142604.2:c.125-2976C>G	NP_001136076.1:n.125-2976C>G
NM_001363695.2:c.144C>G	NP_001350624.1:p.Pro48=