Canonical Allele Identifier: CA2080721401
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924666_27924667delinsAG , CM000675.2:g.27924666_27924667delinsAG GRCh38
NC_000013.10:g.28498803_28498804delinsAG , CM000675.1:g.28498803_28498804delinsAG GRCh37
NC_000013.9:g.27396803_27396804delinsAG NCBI36
NG_008183.1:g.9636_9637delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.817_818delinsAG MANE Select ENSP00000370421.4:p.Ser273=
ENST00000381033.4:c.817_818delinsAG ENSP00000370421.4:p.Ser273=
NM_000209.3:c.817_818delinsAG NP_000200.1:p.Ser273=
NM_000209.4:c.817_818delinsAG MANE Select NP_000200.1:p.Ser273=
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