Canonical Allele Identifier: CA435434104

Gene: UMPS

Linked Data

• gnomAD v4: 3-124737584-A-G
• MyVariant Identifiers: chr3:g.124456431A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737584A>G , CM000665.2:g.124737584A>G	GRCh38
NC_000003.11:g.124456431A>G , CM000665.1:g.124456431A>G	GRCh37
NC_000003.10:g.125939121A>G	NCBI36
NG_017037.1:g.12219A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000232607.7:c.327A>G MANE Select	ENSP00000232607.2:p.Val109=
ENST00000232607.6:c.327A>G	ENSP00000232607.2:p.Val109=
ENST00000460034.5:c.*71A>G	ENSP00000420409.1:n.*71A>G
ENST00000462091.5:c.173A>G	ENSP00000417893.1:p.Ter58Trp
ENST00000467167.5:c.*225A>G	ENSP00000419618.1:n.*225A>G
ENST00000474588.5:c.311-331A>G	ENSP00000420348.1:n.311-331A>G
ENST00000479719.5:c.327A>G	ENSP00000420754.1:p.Val109=
ENST00000497791.5:c.173A>G	ENSP00000419121.1:p.Ter58Trp
ENST00000498715.1:n.45A>G
NM_000373.3:c.327A>G	NP_000364.1:p.Val109=
NR_033434.1:n.279A>G
NR_033437.1:n.532A>G
XR_001740253.2:n.357A>G
NM_000373.4:c.327A>G MANE Select	NP_000364.1:p.Val109=
NR_033434.2:n.193A>G
NR_033437.2:n.446A>G