Canonical Allele Identifier: CA2080721239
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924351A= , CM000675.2:g.27924351A= GRCh38
NC_000013.10:g.28498488A= , CM000675.1:g.28498488A= GRCh37
NC_000013.9:g.27396488A= NCBI36
NG_008183.1:g.9321A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.502A= MANE Select ENSP00000370421.4:p.Asn168=
ENST00000381033.4:c.502A= ENSP00000370421.4:p.Asn168=
NM_000209.3:c.502A= NP_000200.1:p.Asn168=
NM_000209.4:c.502A= MANE Select NP_000200.1:p.Asn168=
Search 100 bp 5'
Search 100 bp 3'