Canonical Allele Identifier: CA1398970951
Gene: UMPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737431A= , CM000665.2:g.124737431A= GRCh38
NC_000003.11:g.124456278A= , CM000665.1:g.124456278A= GRCh37
NC_000003.10:g.125938968A= NCBI36
NG_017037.1:g.12066A=

Transcript Alleles

HGVS Amino-acid change
ENST00000232607.7:c.311-137A= MANE Select ENSP00000232607.2:n.311-137A=
ENST00000232607.6:c.311-137A= ENSP00000232607.2:n.311-137A=
ENST00000460034.5:c.*55-137A= ENSP00000420409.1:n.*55-137A=
ENST00000462091.5:c.157-137A= ENSP00000417893.1:n.157-137A=
ENST00000467167.5:c.*209-137A= ENSP00000419618.1:n.*209-137A=
ENST00000474588.5:c.311-484A= ENSP00000420348.1:n.311-484A=
ENST00000479719.5:c.311-137A= ENSP00000420754.1:n.311-137A=
ENST00000497791.5:c.157-137A= ENSP00000419121.1:n.157-137A=
ENST00000498715.1:n.29-137A=
NM_000373.3:c.311-137A= NP_000364.1:n.311-137A=
NR_033434.1:n.263-137A=
NR_033437.1:n.516-137A=
XR_001740253.2:n.341-137A=
NM_000373.4:c.311-137A= MANE Select NP_000364.1:n.311-137A=
NR_033434.2:n.177-137A=
NR_033437.2:n.430-137A=