Canonical Allele Identifier: CA2080721177
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1957807418

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924232_27924233del , CM000675.2:g.27924232_27924233del GRCh38
NC_000013.10:g.28498369_28498370del , CM000675.1:g.28498369_28498370del GRCh37
NC_000013.9:g.27396369_27396370del NCBI36
NG_008183.1:g.9202_9203del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.407-24_407-23del MANE Select ENSP00000370421.4:n.407-24_407-23del
ENST00000381033.4:c.407-24_407-23del ENSP00000370421.4:n.407-24_407-23del
NM_000209.3:c.407-24_407-23del NP_000200.1:n.407-24_407-23del
XR_941578.1:n.3534-24_3534-23del
XR_941579.1:n.2133-24_2133-23del
XR_941580.1:n.1049-24_1049-23del
XR_941578.2:n.3546-24_3546-23del
XR_941580.2:n.1061-24_1061-23del
NM_000209.4:c.407-24_407-23del MANE Select NP_000200.1:n.407-24_407-23del