Canonical Allele Identifier: CA387645870
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924428G>T , CM000675.2:g.27924428G>T GRCh38
NC_000013.10:g.28498565G>T , CM000675.1:g.28498565G>T GRCh37
NC_000013.9:g.27396565G>T NCBI36
NG_008183.1:g.9398G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.579G>T MANE Select ENSP00000370421.4:p.Trp193Cys
ENST00000381033.4:c.579G>T ENSP00000370421.4:p.Trp193Cys
NM_000209.3:c.579G>T NP_000200.1:p.Trp193Cys
NM_000209.4:c.579G>T MANE Select NP_000200.1:p.Trp193Cys