Canonical Allele Identifier: CA1398970992
Gene: UMPS HGNC NCBI

Linked Data

dbSNP Id: rs1559904865

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.124737504A>G , CM000665.2:g.124737504A>G GRCh38
NC_000003.11:g.124456351A>G , CM000665.1:g.124456351A>G GRCh37
NC_000003.10:g.125939041A>G NCBI36
NG_017037.1:g.12139A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000232607.7:c.311-64A>G MANE Select ENSP00000232607.2:n.311-64A>G
ENST00000232607.6:c.311-64A>G ENSP00000232607.2:n.311-64A>G
ENST00000460034.5:c.*55-64A>G ENSP00000420409.1:n.*55-64A>G
ENST00000462091.5:c.157-64A>G ENSP00000417893.1:n.157-64A>G
ENST00000467167.5:c.*209-64A>G ENSP00000419618.1:n.*209-64A>G
ENST00000474588.5:c.311-411A>G ENSP00000420348.1:n.311-411A>G
ENST00000479719.5:c.311-64A>G ENSP00000420754.1:n.311-64A>G
ENST00000497791.5:c.157-64A>G ENSP00000419121.1:n.157-64A>G
ENST00000498715.1:n.29-64A>G
NM_000373.3:c.311-64A>G NP_000364.1:n.311-64A>G
NR_033434.1:n.263-64A>G
NR_033437.1:n.516-64A>G
XR_001740253.2:n.341-64A>G
NM_000373.4:c.311-64A>G MANE Select NP_000364.1:n.311-64A>G
NR_033434.2:n.177-64A>G
NR_033437.2:n.430-64A>G