Canonical Allele Identifier: CA2622478149
Gene: PDX1 HGNC NCBI

Linked Data

gnomAD v4: 13-27924133-TGGCTCCGGCGGGAGCAGCTGGTAGGGCTAGGGCTCCCTGGCCCCCCTTGAAGGGGTTGGGCTGCGTGGGTGGGGGCTGTGCGG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924142_27924224del , CM000675.2:g.27924142_27924224del GRCh38
NC_000013.10:g.28498279_28498361del , CM000675.1:g.28498279_28498361del GRCh37
NC_000013.9:g.27396279_27396361del NCBI36
NG_008183.1:g.9112_9194del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-114_407-32del MANE Select ENSP00000370421.4:n.407-114_407-32del
ENST00000381033.4:c.407-114_407-32del ENSP00000370421.4:n.407-114_407-32del
NM_000209.3:c.407-114_407-32del NP_000200.1:n.407-114_407-32del
XR_941578.1:n.3534-114_3534-32del
XR_941579.1:n.2133-114_2133-32del
XR_941580.1:n.1049-114_1049-32del
XR_941578.2:n.3546-114_3546-32del
XR_941580.2:n.1061-114_1061-32del
NM_000209.4:c.407-114_407-32del MANE Select NP_000200.1:n.407-114_407-32del
Search 100 bp 5'
Search 100 bp 3'