Canonical Allele Identifier: CA1398971034
Gene: UMPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737594A= , CM000665.2:g.124737594A= GRCh38
NC_000003.11:g.124456441A= , CM000665.1:g.124456441A= GRCh37
NC_000003.10:g.125939131A= NCBI36
NG_017037.1:g.12229A=

Transcript Alleles

HGVS Amino-acid change
ENST00000232607.7:c.337A= MANE Select ENSP00000232607.2:p.Ile113=
ENST00000232607.6:c.337A= ENSP00000232607.2:p.Ile113=
ENST00000460034.5:c.*81A= ENSP00000420409.1:n.*81A=
ENST00000462091.5:c.*9A= ENSP00000417893.1:n.*9A=
ENST00000467167.5:c.*235A= ENSP00000419618.1:n.*235A=
ENST00000474588.5:c.311-321A= ENSP00000420348.1:n.311-321A=
ENST00000479719.5:c.337A= ENSP00000420754.1:p.Ile113=
ENST00000497791.5:c.*9A= ENSP00000419121.1:n.*9A=
ENST00000498715.1:n.55A=
NM_000373.3:c.337A= NP_000364.1:p.Ile113=
NR_033434.1:n.289A=
NR_033437.1:n.542A=
XR_001740253.2:n.367A=
NM_000373.4:c.337A= MANE Select NP_000364.1:p.Ile113=
NR_033434.2:n.203A=
NR_033437.2:n.456A=