Canonical Allele Identifier: CA2667352166

Gene: UMPS

Linked Data

• gnomAD v4: 3-124737442-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737442C>G , CM000665.2:g.124737442C>G	GRCh38
NC_000003.11:g.124456289C>G , CM000665.1:g.124456289C>G	GRCh37
NC_000003.10:g.125938979C>G	NCBI36
NG_017037.1:g.12077C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000232607.7:c.311-126C>G MANE Select	ENSP00000232607.2:n.311-126C>G
ENST00000232607.6:c.311-126C>G	ENSP00000232607.2:n.311-126C>G
ENST00000460034.5:c.*55-126C>G	ENSP00000420409.1:n.*55-126C>G
ENST00000462091.5:c.157-126C>G	ENSP00000417893.1:n.157-126C>G
ENST00000467167.5:c.*209-126C>G	ENSP00000419618.1:n.*209-126C>G
ENST00000474588.5:c.311-473C>G	ENSP00000420348.1:n.311-473C>G
ENST00000479719.5:c.311-126C>G	ENSP00000420754.1:n.311-126C>G
ENST00000497791.5:c.157-126C>G	ENSP00000419121.1:n.157-126C>G
ENST00000498715.1:n.29-126C>G
NM_000373.3:c.311-126C>G	NP_000364.1:n.311-126C>G
NR_033434.1:n.263-126C>G
NR_033437.1:n.516-126C>G
XR_001740253.2:n.341-126C>G
NM_000373.4:c.311-126C>G MANE Select	NP_000364.1:n.311-126C>G
NR_033434.2:n.177-126C>G
NR_033437.2:n.430-126C>G