Canonical Allele Identifier: CA2080721182
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924236A= , CM000675.2:g.27924236A= GRCh38
NC_000013.10:g.28498373A= , CM000675.1:g.28498373A= GRCh37
NC_000013.9:g.27396373A= NCBI36
NG_008183.1:g.9206A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-20A= MANE Select ENSP00000370421.4:n.407-20A=
ENST00000381033.4:c.407-20A= ENSP00000370421.4:n.407-20A=
NM_000209.3:c.407-20A= NP_000200.1:n.407-20A=
XR_941578.1:n.3534-20A=
XR_941579.1:n.2133-20A=
XR_941580.1:n.1049-20A=
XR_941578.2:n.3546-20A=
XR_941580.2:n.1061-20A=
NM_000209.4:c.407-20A= MANE Select NP_000200.1:n.407-20A=
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