Canonical Allele Identifier: CA789823
Gene: PPT1 HGNC NCBI

Linked Data

dbSNP Id: rs545105820
gnomAD v2: 1-40562746-G-A
gnomAD v3: 1-40097074-G-A
gnomAD v4: 1-40097074-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097074G>A , CM000663.2:g.40097074G>A GRCh38
NC_000001.10:g.40562746G>A , CM000663.1:g.40562746G>A GRCh37
NC_000001.9:g.40335333G>A NCBI36
NG_009192.1:g.5397C>T , LRG_690:g.5397C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372779.9:c.128+37C>T ENSP00000361865.5:n.128+37C>T
ENST00000433473.8:c.124+41C>T ENSP00000394863.4:n.124+41C>T
ENST00000439754.6:c.124+41C>T ENSP00000403207.2:n.124+41C>T
ENST00000449045.7:c.124+41C>T ENSP00000392293.2:n.124+41C>T
ENST00000526547.2:c.139C>T
ENST00000527311.7:c.124+41C>T ENSP00000436695.3:n.124+41C>T
ENST00000530704.6:c.124+41C>T ENSP00000431655.1:n.124+41C>T
ENST00000641083.1:c.102+41C>T
ENST00000641236.1:n.136+41C>T
ENST00000641319.1:c.124+41C>T ENSP00000493128.1:n.124+41C>T
ENST00000641471.1:c.124+41C>T ENSP00000493146.1:n.124+41C>T
ENST00000641548.1:c.124+41C>T ENSP00000492984.1:n.124+41C>T
ENST00000641691.1:c.124+41C>T ENSP00000492910.1:n.124+41C>T
ENST00000641924.1:c.124+41C>T ENSP00000493063.1:n.124+41C>T
ENST00000642050.2:c.124+41C>T MANE Select ENSP00000493153.1:n.124+41C>T
ENST00000372779.8:c.124+41C>T ENSP00000361865.4:n.124+41C>T
ENST00000433473.7:c.124+41C>T ENSP00000394863.3:n.124+41C>T
ENST00000449045.6:c.124+41C>T ENSP00000392293.2:n.124+41C>T
ENST00000527311.6:c.124+41C>T ENSP00000436695.2:n.124+41C>T
ENST00000529905.5:c.124+41C>T ENSP00000432053.1:n.124+41C>T
ENST00000530704.5:c.124+41C>T ENSP00000431655.1:n.124+41C>T
NM_000310.3:c.124+41C>T , LRG_690t1:c.124+41C>T NP_000301.1:n.124+41C>T
NM_001142604.1:c.124+41C>T NP_001136076.1:n.124+41C>T
XM_005271008.1:c.124+41C>T XP_005271065.1:n.124+41C>T
NM_001363695.1:c.124+41C>T NP_001350624.1:n.124+41C>T
NM_000310.4:c.124+41C>T MANE Select NP_000301.1:n.124+41C>T
NM_001142604.2:c.124+41C>T NP_001136076.1:n.124+41C>T
NM_001363695.2:c.124+41C>T NP_001350624.1:n.124+41C>T