Canonical Allele Identifier: CA2560451296
Gene: UMPS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737406_124737407insC , CM000665.2:g.124737406_124737407insC GRCh38
NC_000003.11:g.124456253_124456254insC , CM000665.1:g.124456253_124456254insC GRCh37
NC_000003.10:g.125938943_125938944insC NCBI36
NG_017037.1:g.12041_12042insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000232607.7:c.311-162_311-161insC MANE Select ENSP00000232607.2:n.311-162_311-161insC
ENST00000232607.6:c.311-162_311-161insC ENSP00000232607.2:n.311-162_311-161insC
ENST00000460034.5:c.*55-162_*55-161insC ENSP00000420409.1:n.*55-162_*55-161insC
ENST00000462091.5:c.157-162_157-161insC ENSP00000417893.1:n.157-162_157-161insC
ENST00000467167.5:c.*209-162_*209-161insC ENSP00000419618.1:n.*209-162_*209-161insC
ENST00000474588.5:c.311-509_311-508insC ENSP00000420348.1:n.311-509_311-508insC
ENST00000479719.5:c.311-162_311-161insC ENSP00000420754.1:n.311-162_311-161insC
ENST00000497791.5:c.157-162_157-161insC ENSP00000419121.1:n.157-162_157-161insC
ENST00000498715.1:n.29-162_29-161insC
NM_000373.3:c.311-162_311-161insC NP_000364.1:n.311-162_311-161insC
NR_033434.1:n.263-162_263-161insC
NR_033437.1:n.516-162_516-161insC
XR_001740253.2:n.341-162_341-161insC
NM_000373.4:c.311-162_311-161insC MANE Select NP_000364.1:n.311-162_311-161insC
NR_033434.2:n.177-162_177-161insC
NR_033437.2:n.430-162_430-161insC