Canonical Allele Identifier: CA1398971035
Gene: UMPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737596T= , CM000665.2:g.124737596T= GRCh38
NC_000003.11:g.124456443T= , CM000665.1:g.124456443T= GRCh37
NC_000003.10:g.125939133T= NCBI36
NG_017037.1:g.12231T=

Transcript Alleles

HGVS Amino-acid change
ENST00000232607.7:c.339T= MANE Select ENSP00000232607.2:p.Ile113=
ENST00000232607.6:c.339T= ENSP00000232607.2:p.Ile113=
ENST00000460034.5:c.*83T= ENSP00000420409.1:n.*83T=
ENST00000462091.5:c.*11T= ENSP00000417893.1:n.*11T=
ENST00000467167.5:c.*237T= ENSP00000419618.1:n.*237T=
ENST00000474588.5:c.311-319T= ENSP00000420348.1:n.311-319T=
ENST00000479719.5:c.339T= ENSP00000420754.1:p.Ile113=
ENST00000497791.5:c.*11T= ENSP00000419121.1:n.*11T=
ENST00000498715.1:n.57T=
NM_000373.3:c.339T= NP_000364.1:p.Ile113=
NR_033434.1:n.291T=
NR_033437.1:n.544T=
XR_001740253.2:n.369T=
NM_000373.4:c.339T= MANE Select NP_000364.1:p.Ile113=
NR_033434.2:n.205T=
NR_033437.2:n.458T=