Canonical Allele Identifier: CA2080721252
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924386G= , CM000675.2:g.27924386G= GRCh38
NC_000013.10:g.28498523G= , CM000675.1:g.28498523G= GRCh37
NC_000013.9:g.27396523G= NCBI36
NG_008183.1:g.9356G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.537G= MANE Select ENSP00000370421.4:p.Leu179=
ENST00000381033.4:c.537G= ENSP00000370421.4:p.Leu179=
NM_000209.3:c.537G= NP_000200.1:p.Leu179=
NM_000209.4:c.537G= MANE Select NP_000200.1:p.Leu179=