Canonical Allele Identifier: CA697008921
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1258117060

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924464_27924466del , CM000675.2:g.27924464_27924466del GRCh38
NC_000013.10:g.28498601_28498603del , CM000675.1:g.28498601_28498603del GRCh37
NC_000013.9:g.27396601_27396603del NCBI36
NG_008183.1:g.9434_9436del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.615_617del MANE Select ENSP00000370421.4:p.Glu205del
ENST00000381033.4:c.615_617del ENSP00000370421.4:p.Glu205del
NM_000209.3:c.615_617del NP_000200.1:p.Glu205del
NM_000209.4:c.615_617del MANE Select NP_000200.1:p.Glu205del