Canonical Allele Identifier: CA2622478264
Gene: PDX1 HGNC NCBI

Linked Data

gnomAD v4: 13-27924222-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924222C>A , CM000675.2:g.27924222C>A GRCh38
NC_000013.10:g.28498359C>A , CM000675.1:g.28498359C>A GRCh37
NC_000013.9:g.27396359C>A NCBI36
NG_008183.1:g.9192C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-34C>A MANE Select ENSP00000370421.4:n.407-34C>A
ENST00000381033.4:c.407-34C>A ENSP00000370421.4:n.407-34C>A
NM_000209.3:c.407-34C>A NP_000200.1:n.407-34C>A
XR_941578.1:n.3534-34C>A
XR_941579.1:n.2133-34C>A
XR_941580.1:n.1049-34C>A
XR_941578.2:n.3546-34C>A
XR_941580.2:n.1061-34C>A
NM_000209.4:c.407-34C>A MANE Select NP_000200.1:n.407-34C>A
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