Canonical Allele Identifier: CA2080721244
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924364C= , CM000675.2:g.27924364C= GRCh38
NC_000013.10:g.28498501C= , CM000675.1:g.28498501C= GRCh37
NC_000013.9:g.27396501C= NCBI36
NG_008183.1:g.9334C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.515C= MANE Select ENSP00000370421.4:p.Ser172=
ENST00000381033.4:c.515C= ENSP00000370421.4:p.Ser172=
NM_000209.3:c.515C= NP_000200.1:p.Ser172=
NM_000209.4:c.515C= MANE Select NP_000200.1:p.Ser172=
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