Canonical Allele Identifier: CA387645251
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498392G>A (hg19) chr13:g.27924255G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924255G>A , CM000675.2:g.27924255G>A GRCh38
NC_000013.10:g.28498392G>A , CM000675.1:g.28498392G>A GRCh37
NC_000013.9:g.27396392G>A NCBI36
NG_008183.1:g.9225G>A

Transcript Alleles

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