Canonical Allele Identifier: CA2080721476
Gene: PDX1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924822G= , CM000675.2:g.27924822G= GRCh38
NC_000013.10:g.28498959G= , CM000675.1:g.28498959G= GRCh37
NC_000013.9:g.27396959G= NCBI36
NG_008183.1:g.9792G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*121G= MANE Select ENSP00000370421.4:n.*121G=
ENST00000381033.4:c.*121G= ENSP00000370421.4:n.*121G=
NM_000209.3:c.*121G= NP_000200.1:n.*121G=
NM_000209.4:c.*121G= MANE Select NP_000200.1:n.*121G=
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