Canonical Allele Identifier: CA2622478659
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924844A>G , CM000675.2:g.27924844A>G GRCh38
NC_000013.10:g.28498981A>G , CM000675.1:g.28498981A>G GRCh37
NC_000013.9:g.27396981A>G NCBI36
NG_008183.1:g.9814A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*143A>G MANE Select ENSP00000370421.4:n.*143A>G
ENST00000381033.4:c.*143A>G ENSP00000370421.4:n.*143A>G
NM_000209.3:c.*143A>G NP_000200.1:n.*143A>G
NM_000209.4:c.*143A>G MANE Select NP_000200.1:n.*143A>G