Canonical Allele Identifier: CA354272759

Gene: UMPS

Linked Data

• MyVariant Identifiers: chr3:g.124456447C>A (hg19) ; chr3:g.124737600C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737600C>A , CM000665.2:g.124737600C>A	GRCh38
NC_000003.11:g.124456447C>A , CM000665.1:g.124456447C>A	GRCh37
NC_000003.10:g.125939137C>A	NCBI36
NG_017037.1:g.12235C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000232607.7:c.343C>A MANE Select	ENSP00000232607.2:p.Pro115Thr
ENST00000232607.6:c.343C>A	ENSP00000232607.2:p.Pro115Thr
ENST00000460034.5:c.*87C>A	ENSP00000420409.1:n.*87C>A
ENST00000462091.5:c.*15C>A	ENSP00000417893.1:n.*15C>A
ENST00000467167.5:c.*241C>A	ENSP00000419618.1:n.*241C>A
ENST00000474588.5:c.311-315C>A	ENSP00000420348.1:n.311-315C>A
ENST00000479719.5:c.343C>A	ENSP00000420754.1:p.Pro115Thr
ENST00000497791.5:c.*15C>A	ENSP00000419121.1:n.*15C>A
ENST00000498715.1:n.61C>A
NM_000373.3:c.343C>A	NP_000364.1:p.Pro115Thr
NR_033434.1:n.295C>A
NR_033437.1:n.548C>A
XR_001740253.2:n.373C>A
NM_000373.4:c.343C>A MANE Select	NP_000364.1:p.Pro115Thr
NR_033434.2:n.209C>A
NR_033437.2:n.462C>A