Canonical Allele Identifier: CA1000868365
Gene: PPT1 HGNC NCBI

Linked Data

dbSNP Id: rs1649929604

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40097403del , CM000663.2:g.40097403del GRCh38
NC_000001.10:g.40563075del , CM000663.1:g.40563075del GRCh37
NC_000001.9:g.40335662del NCBI36
NG_009192.1:g.5068del , LRG_690:g.5068del

Transcript Alleles

HGVS Amino-acid Change
ENST00000433473.7:c.-165del ENSP00000394863.3:n.-165del
NM_000310.3:c.-165del , LRG_690t1:c.-165del NP_000301.1:n.-165del
NM_001142604.1:c.-165del NP_001136076.1:n.-165del
NM_001363695.1:c.-165del NP_001350624.1:n.-165del