Canonical Allele Identifier: CA483175549

Gene: PDX1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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