Canonical Allele Identifier: CA789784

Gene: PPT1

Linked Data

• ClinVar Variation Id: 382693
• ClinVar RCV Id: RCV000417699 ; RCV001500058 ; RCV003409595
• dbSNP Id: rs200035288
• ExAC: 1:40558106 G / A
• gnomAD v2: 1-40558106-G-A
• gnomAD v3: 1-40092434-G-A
• gnomAD v4: 1-40092434-G-A
• MyVariant Identifiers: chr1:g.40558106G>A (hg19) ; chr1:g.40092434G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092434G>A , CM000663.2:g.40092434G>A	GRCh38
NC_000001.10:g.40558106G>A , CM000663.1:g.40558106G>A	GRCh37
NC_000001.9:g.40330693G>A	NCBI36
NG_009192.1:g.10037C>T , LRG_690:g.10037C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.*34C>T	ENSP00000361865.5:n.*34C>T
ENST00000433473.8:c.195C>T	ENSP00000394863.4:p.Tyr65=
ENST00000439754.6:c.198C>T	ENSP00000403207.2:p.Tyr66=
ENST00000449045.7:c.125-2922C>T	ENSP00000392293.2:n.125-2922C>T
ENST00000526547.2:c.478C>T
ENST00000527311.7:c.198C>T	ENSP00000436695.3:p.Tyr66=
ENST00000530704.6:c.198C>T	ENSP00000431655.1:p.Tyr66=
ENST00000641083.1:c.176C>T
ENST00000641236.1:n.210C>T
ENST00000641319.1:c.198C>T	ENSP00000493128.1:p.Tyr66=
ENST00000641471.1:c.285C>T	ENSP00000493146.1:p.Tyr95=
ENST00000641548.1:c.*50C>T	ENSP00000492984.1:n.*50C>T
ENST00000641691.1:c.*50C>T	ENSP00000492910.1:n.*50C>T
ENST00000641924.1:c.124+4681C>T	ENSP00000493063.1:n.124+4681C>T
ENST00000642050.2:c.198C>T MANE Select	ENSP00000493153.1:p.Tyr66=
ENST00000372779.8:c.285C>T	ENSP00000361865.4:p.Tyr95=
ENST00000433473.7:c.198C>T	ENSP00000394863.3:p.Tyr66=
ENST00000449045.6:c.125-2922C>T	ENSP00000392293.2:n.125-2922C>T
ENST00000526547.1:c.48C>T	ENSP00000436481.1:p.Tyr16=
ENST00000527311.6:c.125-377C>T	ENSP00000436695.2:n.125-377C>T
ENST00000529905.5:c.198C>T	ENSP00000432053.1:p.Tyr66=
ENST00000530704.5:c.198C>T	ENSP00000431655.1:p.Tyr66=
NM_000310.3:c.198C>T , LRG_690t1:c.198C>T	NP_000301.1:p.Tyr66=
NM_001142604.1:c.125-2922C>T	NP_001136076.1:n.125-2922C>T
XM_005271008.1:c.198C>T	XP_005271065.1:p.Tyr66=
NM_001363695.1:c.198C>T	NP_001350624.1:p.Tyr66=
NM_000310.4:c.198C>T MANE Select	NP_000301.1:p.Tyr66=
NM_001142604.2:c.125-2922C>T	NP_001136076.1:n.125-2922C>T
NM_001363695.2:c.198C>T	NP_001350624.1:p.Tyr66=