Canonical Allele Identifier: CA1398971036
Gene: UMPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737597A= , CM000665.2:g.124737597A= GRCh38
NC_000003.11:g.124456444A= , CM000665.1:g.124456444A= GRCh37
NC_000003.10:g.125939134A= NCBI36
NG_017037.1:g.12232A=

Transcript Alleles

HGVS Amino-acid change
ENST00000232607.7:c.340A= MANE Select ENSP00000232607.2:p.Asn114=
ENST00000232607.6:c.340A= ENSP00000232607.2:p.Asn114=
ENST00000460034.5:c.*84A= ENSP00000420409.1:n.*84A=
ENST00000462091.5:c.*12A= ENSP00000417893.1:n.*12A=
ENST00000467167.5:c.*238A= ENSP00000419618.1:n.*238A=
ENST00000474588.5:c.311-318A= ENSP00000420348.1:n.311-318A=
ENST00000479719.5:c.340A= ENSP00000420754.1:p.Asn114=
ENST00000497791.5:c.*12A= ENSP00000419121.1:n.*12A=
ENST00000498715.1:n.58A=
NM_000373.3:c.340A= NP_000364.1:p.Asn114=
NR_033434.1:n.292A=
NR_033437.1:n.545A=
XR_001740253.2:n.370A=
NM_000373.4:c.340A= MANE Select NP_000364.1:p.Asn114=
NR_033434.2:n.206A=
NR_033437.2:n.459A=