Canonical Allele Identifier: CA954374552
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1957813944
gnomAD v3: 13-27924819-C-CG
gnomAD v4: 13-27924819-C-CG
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924823dup , CM000675.2:g.27924823dup GRCh38
NC_000013.10:g.28498960dup , CM000675.1:g.28498960dup GRCh37
NC_000013.9:g.27396960dup NCBI36
NG_008183.1:g.9793dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.*122dup MANE Select ENSP00000370421.4:n.*122dup
ENST00000381033.4:c.*122dup ENSP00000370421.4:n.*122dup
NM_000209.3:c.*122dup NP_000200.1:n.*122dup
NM_000209.4:c.*122dup MANE Select NP_000200.1:n.*122dup
Search 100 bp 5'
Search 100 bp 3'