Canonical Allele Identifier: CA1398970948
Gene: UMPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737427A= , CM000665.2:g.124737427A= GRCh38
NC_000003.11:g.124456274A= , CM000665.1:g.124456274A= GRCh37
NC_000003.10:g.125938964A= NCBI36
NG_017037.1:g.12062A=

Transcript Alleles

HGVS Amino-acid change
ENST00000232607.7:c.311-141A= MANE Select ENSP00000232607.2:n.311-141A=
ENST00000232607.6:c.311-141A= ENSP00000232607.2:n.311-141A=
ENST00000460034.5:c.*55-141A= ENSP00000420409.1:n.*55-141A=
ENST00000462091.5:c.157-141A= ENSP00000417893.1:n.157-141A=
ENST00000467167.5:c.*209-141A= ENSP00000419618.1:n.*209-141A=
ENST00000474588.5:c.311-488A= ENSP00000420348.1:n.311-488A=
ENST00000479719.5:c.311-141A= ENSP00000420754.1:n.311-141A=
ENST00000497791.5:c.157-141A= ENSP00000419121.1:n.157-141A=
ENST00000498715.1:n.29-141A=
NM_000373.3:c.311-141A= NP_000364.1:n.311-141A=
NR_033434.1:n.263-141A=
NR_033437.1:n.516-141A=
XR_001740253.2:n.341-141A=
NM_000373.4:c.311-141A= MANE Select NP_000364.1:n.311-141A=
NR_033434.2:n.177-141A=
NR_033437.2:n.430-141A=