Canonical Allele Identifier: CA387644572

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27920370G>T , CM000675.2:g.27920370G>T GRCh38
NC_000013.10:g.28494507G>T , CM000675.1:g.28494507G>T GRCh37
NC_000013.9:g.27392507G>T NCBI36
NG_008183.1:g.5340G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381033.5:c.232G>T (PDX1) MANE Select ENSP00000370421.4:p.Ala78Ser
ENST00000381033.4:c.232G>T (PDX1) ENSP00000370421.4:p.Ala78Ser
NM_000209.3:c.232G>T (PDX1) NP_000200.1:p.Ala78Ser
NR_047484.1:n.241+794C>A (PLUT)
XR_941578.1:n.377G>T (PDX1)
XR_941579.1:n.377G>T (PDX1)
XR_941580.1:n.377G>T (PDX1)
XR_941578.2:n.389G>T (PDX1)
XR_941580.2:n.389G>T (PDX1)
NM_000209.4:c.232G>T (PDX1) MANE Select NP_000200.1:p.Ala78Ser