Canonical Allele Identifier: CA483175593
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1185624926

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924305C>T , CM000675.2:g.27924305C>T GRCh38
NC_000013.10:g.28498442C>T , CM000675.1:g.28498442C>T GRCh37
NC_000013.9:g.27396442C>T NCBI36
NG_008183.1:g.9275C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.456C>T MANE Select ENSP00000370421.4:p.Ala152=
ENST00000381033.4:c.456C>T ENSP00000370421.4:p.Ala152=
NM_000209.3:c.456C>T NP_000200.1:p.Ala152=
XR_941579.1:n.2182C>T
XR_941580.1:n.1098C>T
XR_941578.2:n.3595C>T
XR_941580.2:n.1110C>T
NM_000209.4:c.456C>T MANE Select NP_000200.1:p.Ala152=