Canonical Allele Identifier: CA483175584

Gene: PDX1

Linked Data

• MyVariant Identifiers: chr13:g.28498439G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27924302G>T , CM000675.2:g.27924302G>T	GRCh38
NC_000013.10:g.28498439G>T , CM000675.1:g.28498439G>T	GRCh37
NC_000013.9:g.27396439G>T	NCBI36
NG_008183.1:g.9272G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381033.5:c.453G>T MANE Select	ENSP00000370421.4:p.Thr151=
ENST00000381033.4:c.453G>T	ENSP00000370421.4:p.Thr151=
NM_000209.3:c.453G>T	NP_000200.1:p.Thr151=
XR_941579.1:n.2179G>T
XR_941580.1:n.1095G>T
XR_941578.2:n.3592G>T
XR_941580.2:n.1107G>T
NM_000209.4:c.453G>T MANE Select	NP_000200.1:p.Thr151=