Canonical Allele Identifier: CA2739272470
Gene: PPT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2846029
ClinVar RCV Id: RCV003621221

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.40078645_40078661del , CM000663.2:g.40078645_40078661del GRCh38
NC_000001.10:g.40544317_40544333del , CM000663.1:g.40544317_40544333del GRCh37
NC_000001.9:g.40316904_40316920del NCBI36
NG_009192.1:g.23811_23827del , LRG_690:g.23811_23827del

Transcript Alleles

HGVS Amino-acid change
ENST00000433473.8:c.625-2_639del
ENST00000439754.6:c.628-2_642del
ENST00000449045.7:c.319-2_333del
ENST00000527311.7:c.397-2_411del
ENST00000530076.6:c.-30-2_-16del
ENST00000530704.6:c.*251-2_*265del
ENST00000641083.1:c.606-2_620del
ENST00000641236.1:n.865-2_879del
ENST00000641319.1:c.628-2_642del
ENST00000641381.1:c.149-1747_149-1731del
ENST00000641471.1:c.715-2_729del
ENST00000641691.1:c.*480-2_*494del
ENST00000641924.1:c.*57-2_*71del
ENST00000642050.2:c.628-2_642del
ENST00000372775.2:n.25-2_39del
ENST00000372779.8:c.715-2_729del
ENST00000433473.7:c.628-2_642del
ENST00000439754.5:c.313-2_327del
ENST00000449045.6:c.319-2_333del
ENST00000527311.6:c.403-2_417del
ENST00000529905.5:c.628-2_642del
ENST00000530076.5:c.-30-2_-16del
ENST00000530704.5:c.*251-2_*265del
NM_000310.3:c.628-2_642del , LRG_690t1:c.628-2_642del
NM_001142604.1:c.319-2_333del
XM_005271008.1:c.628-2_642del
NM_001363695.1:c.628-2_642del
NM_000310.4:c.628-2_642del
NM_001142604.2:c.319-2_333del
NM_001363695.2:c.628-2_642del