Canonical Allele Identifier: CA387645332
Gene: PDX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.28498431A>C (hg19) chr13:g.27924294A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924294A>C , CM000675.2:g.27924294A>C GRCh38
NC_000013.10:g.28498431A>C , CM000675.1:g.28498431A>C GRCh37
NC_000013.9:g.27396431A>C NCBI36
NG_008183.1:g.9264A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.445A>C MANE Select ENSP00000370421.4:p.Thr149Pro
ENST00000381033.4:c.445A>C ENSP00000370421.4:p.Thr149Pro
NM_000209.3:c.445A>C NP_000200.1:p.Thr149Pro
XR_941578.1:n.3572A>C
XR_941579.1:n.2171A>C
XR_941580.1:n.1087A>C
XR_941578.2:n.3584A>C
XR_941580.2:n.1099A>C
NM_000209.4:c.445A>C MANE Select NP_000200.1:p.Thr149Pro
Search 100 bp 5'
Search 100 bp 3'