Canonical Allele Identifier: CA387643190

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920143A>C , CM000675.2:g.27920143A>C GRCh38
NC_000013.10:g.28494280A>C , CM000675.1:g.28494280A>C GRCh37
NC_000013.9:g.27392280A>C NCBI36
NG_008183.1:g.5113A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.5A>C (PDX1) MANE Select ENSP00000370421.4:p.Asn2Thr
ENST00000381033.4:c.5A>C (PDX1) ENSP00000370421.4:p.Asn2Thr
NM_000209.3:c.5A>C (PDX1) NP_000200.1:p.Asn2Thr
NR_047484.1:n.241+1021T>G (PLUT)
XR_941578.1:n.150A>C (PDX1)
XR_941579.1:n.150A>C (PDX1)
XR_941580.1:n.150A>C (PDX1)
XR_941578.2:n.162A>C (PDX1)
XR_941580.2:n.162A>C (PDX1)
NM_000209.4:c.5A>C (PDX1) MANE Select NP_000200.1:p.Asn2Thr