Canonical Allele Identifier: CA483175565
Gene: PDX1 HGNC NCBI

Linked Data

COSMIC: COSM5362261
MyVariant Identifiers: chr13:g.28498433G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924296G>A , CM000675.2:g.27924296G>A GRCh38
NC_000013.10:g.28498433G>A , CM000675.1:g.28498433G>A GRCh37
NC_000013.9:g.27396433G>A NCBI36
NG_008183.1:g.9266G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.447G>A MANE Select ENSP00000370421.4:p.Thr149=
ENST00000381033.4:c.447G>A ENSP00000370421.4:p.Thr149=
NM_000209.3:c.447G>A NP_000200.1:p.Thr149=
XR_941578.1:n.3574G>A
XR_941579.1:n.2173G>A
XR_941580.1:n.1089G>A
XR_941578.2:n.3586G>A
XR_941580.2:n.1101G>A
NM_000209.4:c.447G>A MANE Select NP_000200.1:p.Thr149=
Search 100 bp 5'
Search 100 bp 3'