Canonical Allele Identifier: CA2080721376
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924620A= , CM000675.2:g.27924620A= GRCh38
NC_000013.10:g.28498757A= , CM000675.1:g.28498757A= GRCh37
NC_000013.9:g.27396757A= NCBI36
NG_008183.1:g.9590A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.771A= MANE Select ENSP00000370421.4:p.Arg257=
ENST00000381033.4:c.771A= ENSP00000370421.4:p.Arg257=
NM_000209.3:c.771A= NP_000200.1:p.Arg257=
NM_000209.4:c.771A= MANE Select NP_000200.1:p.Arg257=
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Search 100 bp 3'