Canonical Allele Identifier: CA387645420
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498474A>C (hg19) chr13:g.27924337A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924337A>C , CM000675.2:g.27924337A>C GRCh38
NC_000013.10:g.28498474A>C , CM000675.1:g.28498474A>C GRCh37
NC_000013.9:g.27396474A>C NCBI36
NG_008183.1:g.9307A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.488A>C MANE Select ENSP00000370421.4:p.Lys163Thr
ENST00000381033.4:c.488A>C ENSP00000370421.4:p.Lys163Thr
NM_000209.3:c.488A>C NP_000200.1:p.Lys163Thr
NM_000209.4:c.488A>C MANE Select NP_000200.1:p.Lys163Thr
Search 100 bp 5'
Search 100 bp 3'