Canonical Allele Identifier: CA263468

Gene: PPT1

Linked Data

• ClinVar Variation Id: 56175
• ClinVar RCV Id: RCV000049586
• dbSNP Id: rs386833627
• MyVariant Identifiers: chr1:g.40562794A>T (hg19) ; chr1:g.40097122A>T (hg38)
• PubMed: PMID:21990111

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40097122A>T , CM000663.2:g.40097122A>T	GRCh38
NC_000001.10:g.40562794A>T , CM000663.1:g.40562794A>T	GRCh37
NC_000001.9:g.40335381A>T	NCBI36
NG_009192.1:g.5349T>A , LRG_690:g.5349T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.117T>A	ENSP00000361865.5:p.His39Gln
ENST00000433473.8:c.117T>A	ENSP00000394863.4:p.His39Gln
ENST00000439754.6:c.117T>A	ENSP00000403207.2:p.His39Gln
ENST00000449045.7:c.117T>A	ENSP00000392293.2:p.His39Gln
ENST00000526547.2:c.91T>A
ENST00000527311.7:c.117T>A	ENSP00000436695.3:p.His39Gln
ENST00000530704.6:c.117T>A	ENSP00000431655.1:p.His39Gln
ENST00000641083.1:c.95T>A
ENST00000641236.1:n.129T>A
ENST00000641319.1:c.117T>A	ENSP00000493128.1:p.His39Gln
ENST00000641471.1:c.117T>A	ENSP00000493146.1:p.His39Gln
ENST00000641548.1:c.117T>A	ENSP00000492984.1:p.His39Gln
ENST00000641691.1:c.117T>A	ENSP00000492910.1:p.His39Gln
ENST00000641924.1:c.117T>A	ENSP00000493063.1:p.His39Gln
ENST00000642050.2:c.117T>A MANE Select	ENSP00000493153.1:p.His39Gln
ENST00000372779.8:c.117T>A	ENSP00000361865.4:p.His39Gln
ENST00000433473.7:c.117T>A	ENSP00000394863.3:p.His39Gln
ENST00000449045.6:c.117T>A	ENSP00000392293.2:p.His39Gln
ENST00000527311.6:c.117T>A	ENSP00000436695.2:p.His39Gln
ENST00000529905.5:c.117T>A	ENSP00000432053.1:p.His39Gln
ENST00000530704.5:c.117T>A	ENSP00000431655.1:p.His39Gln
NM_000310.3:c.117T>A , LRG_690t1:c.117T>A	NP_000301.1:p.His39Gln
NM_001142604.1:c.117T>A	NP_001136076.1:p.His39Gln
XM_005271008.1:c.117T>A	XP_005271065.1:p.His39Gln
NM_001363695.1:c.117T>A	NP_001350624.1:p.His39Gln
NM_000310.4:c.117T>A MANE Select	NP_000301.1:p.His39Gln
NM_001142604.2:c.117T>A	NP_001136076.1:p.His39Gln
NM_001363695.2:c.117T>A	NP_001350624.1:p.His39Gln