Canonical Allele Identifier: CA2622478285
Gene: PDX1 HGNC NCBI

Linked Data

gnomAD v4: 13-27924243-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924243G>T , CM000675.2:g.27924243G>T GRCh38
NC_000013.10:g.28498380G>T , CM000675.1:g.28498380G>T GRCh37
NC_000013.9:g.27396380G>T NCBI36
NG_008183.1:g.9213G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.407-13G>T MANE Select ENSP00000370421.4:n.407-13G>T
ENST00000381033.4:c.407-13G>T ENSP00000370421.4:n.407-13G>T
NM_000209.3:c.407-13G>T NP_000200.1:n.407-13G>T
XR_941578.1:n.3534-13G>T
XR_941579.1:n.2133-13G>T
XR_941580.1:n.1049-13G>T
XR_941578.2:n.3546-13G>T
XR_941580.2:n.1061-13G>T
NM_000209.4:c.407-13G>T MANE Select NP_000200.1:n.407-13G>T
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Search 100 bp 3'