Canonical Allele Identifier: CA2080721490
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924842G= , CM000675.2:g.27924842G= GRCh38
NC_000013.10:g.28498979G= , CM000675.1:g.28498979G= GRCh37
NC_000013.9:g.27396979G= NCBI36
NG_008183.1:g.9812G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*141G= MANE Select ENSP00000370421.4:n.*141G=
ENST00000381033.4:c.*141G= ENSP00000370421.4:n.*141G=
NM_000209.3:c.*141G= NP_000200.1:n.*141G=
NM_000209.4:c.*141G= MANE Select NP_000200.1:n.*141G=
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