Canonical Allele Identifier: CA2080721485
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1957814051

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924828_27924831del , CM000675.2:g.27924828_27924831del GRCh38
NC_000013.10:g.28498965_28498968del , CM000675.1:g.28498965_28498968del GRCh37
NC_000013.9:g.27396965_27396968del NCBI36
NG_008183.1:g.9798_9801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*127_*130del MANE Select ENSP00000370421.4:n.*127_*130del
ENST00000381033.4:c.*127_*130del ENSP00000370421.4:n.*127_*130del
NM_000209.3:c.*127_*130del NP_000200.1:n.*127_*130del
NM_000209.4:c.*127_*130del MANE Select NP_000200.1:n.*127_*130del