Canonical Allele Identifier: CA2080721457
Gene: PDX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924789C= , CM000675.2:g.27924789C= GRCh38
NC_000013.10:g.28498926C= , CM000675.1:g.28498926C= GRCh37
NC_000013.9:g.27396926C= NCBI36
NG_008183.1:g.9759C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*88C= MANE Select ENSP00000370421.4:n.*88C=
ENST00000381033.4:c.*88C= ENSP00000370421.4:n.*88C=
NM_000209.3:c.*88C= NP_000200.1:n.*88C=
NM_000209.4:c.*88C= MANE Select NP_000200.1:n.*88C=