Canonical Allele Identifier: CA1398971050
Gene: UMPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737642G= , CM000665.2:g.124737642G= GRCh38
NC_000003.11:g.124456489G= , CM000665.1:g.124456489G= GRCh37
NC_000003.10:g.125939179G= NCBI36
NG_017037.1:g.12277G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000232607.7:c.385G= MANE Select ENSP00000232607.2:p.Gly129=
ENST00000232607.6:c.385G= ENSP00000232607.2:p.Gly129=
ENST00000460034.5:c.*129G= ENSP00000420409.1:n.*129G=
ENST00000462091.5:c.*57G= ENSP00000417893.1:n.*57G=
ENST00000467167.5:c.*283G= ENSP00000419618.1:n.*283G=
ENST00000474588.5:c.311-273G= ENSP00000420348.1:n.311-273G=
ENST00000479719.5:c.385G= ENSP00000420754.1:p.Gly129=
ENST00000497791.5:c.*57G= ENSP00000419121.1:n.*57G=
ENST00000498715.1:n.103G=
NM_000373.3:c.385G= NP_000364.1:p.Gly129=
NR_033434.1:n.337G=
NR_033437.1:n.590G=
XR_001740253.2:n.415G=
NM_000373.4:c.385G= MANE Select NP_000364.1:p.Gly129=
NR_033434.2:n.251G=
NR_033437.2:n.504G=