Canonical Allele Identifier: CA387645356
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498443T>G (hg19) chr13:g.27924306T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924306T>G , CM000675.2:g.27924306T>G GRCh38
NC_000013.10:g.28498443T>G , CM000675.1:g.28498443T>G GRCh37
NC_000013.9:g.27396443T>G NCBI36
NG_008183.1:g.9276T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.457T>G MANE Select ENSP00000370421.4:p.Tyr153Asp
ENST00000381033.4:c.457T>G ENSP00000370421.4:p.Tyr153Asp
NM_000209.3:c.457T>G NP_000200.1:p.Tyr153Asp
XR_941579.1:n.2183T>G
XR_941580.1:n.1099T>G
XR_941580.2:n.1111T>G
NM_000209.4:c.457T>G MANE Select NP_000200.1:p.Tyr153Asp
Search 100 bp 5'
Search 100 bp 3'