Canonical Allele Identifier: CA387645342
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924298G>C , CM000675.2:g.27924298G>C GRCh38
NC_000013.10:g.28498435G>C , CM000675.1:g.28498435G>C GRCh37
NC_000013.9:g.27396435G>C NCBI36
NG_008183.1:g.9268G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.449G>C MANE Select ENSP00000370421.4:p.Arg150Pro
ENST00000381033.4:c.449G>C ENSP00000370421.4:p.Arg150Pro
NM_000209.3:c.449G>C NP_000200.1:p.Arg150Pro
XR_941578.1:n.3576G>C
XR_941579.1:n.2175G>C
XR_941580.1:n.1091G>C
XR_941578.2:n.3588G>C
XR_941580.2:n.1103G>C
NM_000209.4:c.449G>C MANE Select NP_000200.1:p.Arg150Pro