Canonical Allele Identifier: CA483175652
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498469G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924332G>A , CM000675.2:g.27924332G>A GRCh38
NC_000013.10:g.28498469G>A , CM000675.1:g.28498469G>A GRCh37
NC_000013.9:g.27396469G>A NCBI36
NG_008183.1:g.9302G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.483G>A MANE Select ENSP00000370421.4:p.Leu161=
ENST00000381033.4:c.483G>A ENSP00000370421.4:p.Leu161=
NM_000209.3:c.483G>A NP_000200.1:p.Leu161=
XR_941580.1:n.1125G>A
XR_941580.2:n.1137G>A
NM_000209.4:c.483G>A MANE Select NP_000200.1:p.Leu161=
Search 100 bp 5'
Search 100 bp 3'