Canonical Allele Identifier: CA387643845

Linked Data

dbSNP Id: rs1957772368

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920238G>C , CM000675.2:g.27920238G>C GRCh38
NC_000013.10:g.28494375G>C , CM000675.1:g.28494375G>C GRCh37
NC_000013.9:g.27392375G>C NCBI36
NG_008183.1:g.5208G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000381033.5:c.100G>C (PDX1) MANE Select ENSP00000370421.4:p.Ala34Pro
ENST00000381033.4:c.100G>C (PDX1) ENSP00000370421.4:p.Ala34Pro
NM_000209.3:c.100G>C (PDX1) NP_000200.1:p.Ala34Pro
NR_047484.1:n.241+926C>G (PLUT)
XR_941578.1:n.245G>C (PDX1)
XR_941579.1:n.245G>C (PDX1)
XR_941580.1:n.245G>C (PDX1)
XR_941578.2:n.257G>C (PDX1)
XR_941580.2:n.257G>C (PDX1)
NM_000209.4:c.100G>C (PDX1) MANE Select NP_000200.1:p.Ala34Pro