Canonical Allele Identifier: CA387645836
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924423A>C , CM000675.2:g.27924423A>C GRCh38
NC_000013.10:g.28498560A>C , CM000675.1:g.28498560A>C GRCh37
NC_000013.9:g.27396560A>C NCBI36
NG_008183.1:g.9393A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.574A>C MANE Select ENSP00000370421.4:p.Ile192Leu
ENST00000381033.4:c.574A>C ENSP00000370421.4:p.Ile192Leu
NM_000209.3:c.574A>C NP_000200.1:p.Ile192Leu
NM_000209.4:c.574A>C MANE Select NP_000200.1:p.Ile192Leu