Canonical Allele Identifier: CA2622478280
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924239C>T , CM000675.2:g.27924239C>T GRCh38
NC_000013.10:g.28498376C>T , CM000675.1:g.28498376C>T GRCh37
NC_000013.9:g.27396376C>T NCBI36
NG_008183.1:g.9209C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.407-17C>T MANE Select ENSP00000370421.4:n.407-17C>T
ENST00000381033.4:c.407-17C>T ENSP00000370421.4:n.407-17C>T
NM_000209.3:c.407-17C>T NP_000200.1:n.407-17C>T
XR_941578.1:n.3534-17C>T
XR_941579.1:n.2133-17C>T
XR_941580.1:n.1049-17C>T
XR_941578.2:n.3546-17C>T
XR_941580.2:n.1061-17C>T
NM_000209.4:c.407-17C>T MANE Select NP_000200.1:n.407-17C>T