Canonical Allele Identifier: CA387645990
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498584A>T (hg19) chr13:g.27924447A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924447A>T , CM000675.2:g.27924447A>T GRCh38
NC_000013.10:g.28498584A>T , CM000675.1:g.28498584A>T GRCh37
NC_000013.9:g.27396584A>T NCBI36
NG_008183.1:g.9417A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.598A>T MANE Select ENSP00000370421.4:p.Lys200Ter
ENST00000381033.4:c.598A>T ENSP00000370421.4:p.Lys200Ter
NM_000209.3:c.598A>T NP_000200.1:p.Lys200Ter
NM_000209.4:c.598A>T MANE Select NP_000200.1:p.Lys200Ter
Search 100 bp 5'
Search 100 bp 3'