Canonical Allele Identifier: CA697008263
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1364450893

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924235C>T , CM000675.2:g.27924235C>T GRCh38
NC_000013.10:g.28498372C>T , CM000675.1:g.28498372C>T GRCh37
NC_000013.9:g.27396372C>T NCBI36
NG_008183.1:g.9205C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-21C>T MANE Select ENSP00000370421.4:n.407-21C>T
ENST00000381033.4:c.407-21C>T ENSP00000370421.4:n.407-21C>T
NM_000209.3:c.407-21C>T NP_000200.1:n.407-21C>T
XR_941578.1:n.3534-21C>T
XR_941579.1:n.2133-21C>T
XR_941580.1:n.1049-21C>T
XR_941578.2:n.3546-21C>T
XR_941580.2:n.1061-21C>T
NM_000209.4:c.407-21C>T MANE Select NP_000200.1:n.407-21C>T