Canonical Allele Identifier: CA354272807

Gene: UMPS

Linked Data

• gnomAD v4: 3-124737609-A-G
• MyVariant Identifiers: chr3:g.124456456A>G (hg19) ; chr3:g.124737609A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737609A>G , CM000665.2:g.124737609A>G	GRCh38
NC_000003.11:g.124456456A>G , CM000665.1:g.124456456A>G	GRCh37
NC_000003.10:g.125939146A>G	NCBI36
NG_017037.1:g.12244A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232607.7:c.352A>G MANE Select	ENSP00000232607.2:p.Thr118Ala
ENST00000232607.6:c.352A>G	ENSP00000232607.2:p.Thr118Ala
ENST00000460034.5:c.*96A>G	ENSP00000420409.1:n.*96A>G
ENST00000462091.5:c.*24A>G	ENSP00000417893.1:n.*24A>G
ENST00000467167.5:c.*250A>G	ENSP00000419618.1:n.*250A>G
ENST00000474588.5:c.311-306A>G	ENSP00000420348.1:n.311-306A>G
ENST00000479719.5:c.352A>G	ENSP00000420754.1:p.Thr118Ala
ENST00000497791.5:c.*24A>G	ENSP00000419121.1:n.*24A>G
ENST00000498715.1:n.70A>G
NM_000373.3:c.352A>G	NP_000364.1:p.Thr118Ala
NR_033434.1:n.304A>G
NR_033437.1:n.557A>G
XR_001740253.2:n.382A>G
NM_000373.4:c.352A>G MANE Select	NP_000364.1:p.Thr118Ala
NR_033434.2:n.218A>G
NR_033437.2:n.471A>G