Canonical Allele Identifier: CA2080721422
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924700G= , CM000675.2:g.27924700G= GRCh38
NC_000013.10:g.28498837G= , CM000675.1:g.28498837G= GRCh37
NC_000013.9:g.27396837G= NCBI36
NG_008183.1:g.9670G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.851G= MANE Select ENSP00000370421.4:p.Ter284=
ENST00000381033.4:c.851G= ENSP00000370421.4:p.Ter284=
NM_000209.3:c.851G= NP_000200.1:p.Ter284=
NM_000209.4:c.851G= MANE Select NP_000200.1:p.Ter284=
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