Canonical Allele Identifier: CA387645888
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924430T>C , CM000675.2:g.27924430T>C GRCh38
NC_000013.10:g.28498567T>C , CM000675.1:g.28498567T>C GRCh37
NC_000013.9:g.27396567T>C NCBI36
NG_008183.1:g.9400T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.581T>C MANE Select ENSP00000370421.4:p.Phe194Ser
ENST00000381033.4:c.581T>C ENSP00000370421.4:p.Phe194Ser
NM_000209.3:c.581T>C NP_000200.1:p.Phe194Ser
NM_000209.4:c.581T>C MANE Select NP_000200.1:p.Phe194Ser