Canonical Allele Identifier: CA2622478356
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924729dup , CM000675.2:g.27924729dup GRCh38
NC_000013.10:g.28498866dup , CM000675.1:g.28498866dup GRCh37
NC_000013.9:g.27396866dup NCBI36
NG_008183.1:g.9699dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*28dup MANE Select ENSP00000370421.4:n.*28dup
ENST00000381033.4:c.*28dup ENSP00000370421.4:n.*28dup
NM_000209.3:c.*28dup NP_000200.1:n.*28dup
NM_000209.4:c.*28dup MANE Select NP_000200.1:n.*28dup