Canonical Allele Identifier: CA483175551

Gene: PDX1

Linked Data

• MyVariant Identifiers: chr13:g.28498409G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27924272G>T , CM000675.2:g.27924272G>T	GRCh38
NC_000013.10:g.28498409G>T , CM000675.1:g.28498409G>T	GRCh37
NC_000013.9:g.27396409G>T	NCBI36
NG_008183.1:g.9242G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381033.5:c.423G>T MANE Select	ENSP00000370421.4:p.Ala141=
ENST00000381033.4:c.423G>T	ENSP00000370421.4:p.Ala141=
NM_000209.3:c.423G>T	NP_000200.1:p.Ala141=
XR_941578.1:n.3550G>T
XR_941579.1:n.2149G>T
XR_941580.1:n.1065G>T
XR_941578.2:n.3562G>T
XR_941580.2:n.1077G>T
NM_000209.4:c.423G>T MANE Select	NP_000200.1:p.Ala141=