Canonical Allele Identifier: CA1398970997
Gene: UMPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737515C= , CM000665.2:g.124737515C= GRCh38
NC_000003.11:g.124456362C= , CM000665.1:g.124456362C= GRCh37
NC_000003.10:g.125939052C= NCBI36
NG_017037.1:g.12150C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000232607.7:c.311-53C= MANE Select ENSP00000232607.2:n.311-53C=
ENST00000232607.6:c.311-53C= ENSP00000232607.2:n.311-53C=
ENST00000460034.5:c.*55-53C= ENSP00000420409.1:n.*55-53C=
ENST00000462091.5:c.157-53C= ENSP00000417893.1:n.157-53C=
ENST00000467167.5:c.*209-53C= ENSP00000419618.1:n.*209-53C=
ENST00000474588.5:c.311-400C= ENSP00000420348.1:n.311-400C=
ENST00000479719.5:c.311-53C= ENSP00000420754.1:n.311-53C=
ENST00000497791.5:c.157-53C= ENSP00000419121.1:n.157-53C=
ENST00000498715.1:n.29-53C=
NM_000373.3:c.311-53C= NP_000364.1:n.311-53C=
NR_033434.1:n.263-53C=
NR_033437.1:n.516-53C=
XR_001740253.2:n.341-53C=
NM_000373.4:c.311-53C= MANE Select NP_000364.1:n.311-53C=
NR_033434.2:n.177-53C=
NR_033437.2:n.430-53C=