Canonical Allele Identifier: CA387646874
Gene: PDX1 HGNC NCBI

Linked Data

dbSNP Id: rs1482175613

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27924672G>C , CM000675.2:g.27924672G>C GRCh38
NC_000013.10:g.28498809G>C , CM000675.1:g.28498809G>C GRCh37
NC_000013.9:g.27396809G>C NCBI36
NG_008183.1:g.9642G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.823G>C MANE Select ENSP00000370421.4:p.Ala275Pro
ENST00000381033.4:c.823G>C ENSP00000370421.4:p.Ala275Pro
NM_000209.3:c.823G>C NP_000200.1:p.Ala275Pro
NM_000209.4:c.823G>C MANE Select NP_000200.1:p.Ala275Pro