Canonical Allele Identifier: CA2080721174
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924226G= , CM000675.2:g.27924226G= GRCh38
NC_000013.10:g.28498363G= , CM000675.1:g.28498363G= GRCh37
NC_000013.9:g.27396363G= NCBI36
NG_008183.1:g.9196G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-30G= MANE Select ENSP00000370421.4:n.407-30G=
ENST00000381033.4:c.407-30G= ENSP00000370421.4:n.407-30G=
NM_000209.3:c.407-30G= NP_000200.1:n.407-30G=
XR_941578.1:n.3534-30G=
XR_941579.1:n.2133-30G=
XR_941580.1:n.1049-30G=
XR_941578.2:n.3546-30G=
XR_941580.2:n.1061-30G=
NM_000209.4:c.407-30G= MANE Select NP_000200.1:n.407-30G=
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