Canonical Allele Identifier: CA483175519

Gene: PDX1

Linked Data

• MyVariant Identifiers: chr13:g.28498394C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27924257C>A , CM000675.2:g.27924257C>A	GRCh38
NC_000013.10:g.28498394C>A , CM000675.1:g.28498394C>A	GRCh37
NC_000013.9:g.27396394C>A	NCBI36
NG_008183.1:g.9227C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381033.5:c.408C>A MANE Select	ENSP00000370421.4:p.Gly136=
ENST00000381033.4:c.408C>A	ENSP00000370421.4:p.Gly136=
NM_000209.3:c.408C>A	NP_000200.1:p.Gly136=
XR_941578.1:n.3535C>A
XR_941579.1:n.2134C>A
XR_941580.1:n.1050C>A
XR_941578.2:n.3547C>A
XR_941580.2:n.1062C>A
NM_000209.4:c.408C>A MANE Select	NP_000200.1:p.Gly136=