Canonical Allele Identifier: CA387643524

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920182A>T , CM000675.2:g.27920182A>T GRCh38
NC_000013.10:g.28494319A>T , CM000675.1:g.28494319A>T GRCh37
NC_000013.9:g.27392319A>T NCBI36
NG_008183.1:g.5152A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.44A>T (PDX1) MANE Select ENSP00000370421.4:p.Lys15Met
ENST00000381033.4:c.44A>T (PDX1) ENSP00000370421.4:p.Lys15Met
NM_000209.3:c.44A>T (PDX1) NP_000200.1:p.Lys15Met
NR_047484.1:n.241+982T>A (PLUT)
XR_941578.1:n.189A>T (PDX1)
XR_941579.1:n.189A>T (PDX1)
XR_941580.1:n.189A>T (PDX1)
XR_941578.2:n.201A>T (PDX1)
XR_941580.2:n.201A>T (PDX1)
NM_000209.4:c.44A>T (PDX1) MANE Select NP_000200.1:p.Lys15Met