Canonical Allele Identifier: CA387646155

Gene: PDX1

Linked Data

• gnomAD v4: 13-27924477-G-A
• MyVariant Identifiers: chr13:g.28498614G>A (hg19) ; chr13:g.27924477G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27924477G>A , CM000675.2:g.27924477G>A	GRCh38
NC_000013.10:g.28498614G>A , CM000675.1:g.28498614G>A	GRCh37
NC_000013.9:g.27396614G>A	NCBI36
NG_008183.1:g.9447G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381033.5:c.628G>A MANE Select	ENSP00000370421.4:p.Gly210Ser
ENST00000381033.4:c.628G>A	ENSP00000370421.4:p.Gly210Ser
NM_000209.3:c.628G>A	NP_000200.1:p.Gly210Ser
NM_000209.4:c.628G>A MANE Select	NP_000200.1:p.Gly210Ser