Canonical Allele Identifier: CA387645334
Gene: PDX1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.445A>T MANE Select ENSP00000370421.4:p.Thr149Ser
ENST00000381033.4:c.445A>T ENSP00000370421.4:p.Thr149Ser
NM_000209.3:c.445A>T NP_000200.1:p.Thr149Ser
XR_941578.1:n.3572A>T
XR_941579.1:n.2171A>T
XR_941580.1:n.1087A>T
XR_941578.2:n.3584A>T
XR_941580.2:n.1099A>T
NM_000209.4:c.445A>T MANE Select NP_000200.1:p.Thr149Ser