Canonical Allele Identifier: CA2645092861

Gene: PPT1

Linked Data

• gnomAD v4: 1-40092578-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40092578C>A , CM000663.2:g.40092578C>A	GRCh38
NC_000001.10:g.40558250C>A , CM000663.1:g.40558250C>A	GRCh37
NC_000001.9:g.40330837C>A	NCBI36
NG_009192.1:g.9893G>T , LRG_690:g.9893G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372779.9:c.129-71G>T	ENSP00000361865.5:n.129-71G>T
ENST00000433473.8:c.125-74G>T	ENSP00000394863.4:n.125-74G>T
ENST00000439754.6:c.125-71G>T	ENSP00000403207.2:n.125-71G>T
ENST00000449045.7:c.125-3066G>T	ENSP00000392293.2:n.125-3066G>T
ENST00000526547.2:c.405-71G>T
ENST00000527311.7:c.125-71G>T	ENSP00000436695.3:n.125-71G>T
ENST00000530704.6:c.125-71G>T	ENSP00000431655.1:n.125-71G>T
ENST00000641083.1:c.103-71G>T
ENST00000641236.1:n.137-71G>T
ENST00000641319.1:c.125-71G>T	ENSP00000493128.1:n.125-71G>T
ENST00000641471.1:c.212-71G>T	ENSP00000493146.1:n.212-71G>T
ENST00000641548.1:c.125-78G>T	ENSP00000492984.1:n.125-78G>T
ENST00000641691.1:c.125-78G>T	ENSP00000492910.1:n.125-78G>T
ENST00000641924.1:c.124+4537G>T	ENSP00000493063.1:n.124+4537G>T
ENST00000642050.2:c.125-71G>T MANE Select	ENSP00000493153.1:n.125-71G>T
ENST00000372779.8:c.212-71G>T	ENSP00000361865.4:n.212-71G>T
ENST00000433473.7:c.125-71G>T	ENSP00000394863.3:n.125-71G>T
ENST00000449045.6:c.125-3066G>T	ENSP00000392293.2:n.125-3066G>T
ENST00000526547.1:c.-26-71G>T	ENSP00000436481.1:n.-26-71G>T
ENST00000527311.6:c.125-521G>T	ENSP00000436695.2:n.125-521G>T
ENST00000529905.5:c.125-71G>T	ENSP00000432053.1:n.125-71G>T
ENST00000530704.5:c.125-71G>T	ENSP00000431655.1:n.125-71G>T
NM_000310.3:c.125-71G>T , LRG_690t1:c.125-71G>T	NP_000301.1:n.125-71G>T
NM_001142604.1:c.125-3066G>T	NP_001136076.1:n.125-3066G>T
XM_005271008.1:c.125-71G>T	XP_005271065.1:n.125-71G>T
NM_001363695.1:c.125-71G>T	NP_001350624.1:n.125-71G>T
NM_000310.4:c.125-71G>T MANE Select	NP_000301.1:n.125-71G>T
NM_001142604.2:c.125-3066G>T	NP_001136076.1:n.125-3066G>T
NM_001363695.2:c.125-71G>T	NP_001350624.1:n.125-71G>T