Canonical Allele Identifier: CA435434602

Gene: UMPS

Linked Data

• MyVariant Identifiers: chr3:g.124456596G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737749G>A , CM000665.2:g.124737749G>A	GRCh38
NC_000003.11:g.124456596G>A , CM000665.1:g.124456596G>A	GRCh37
NC_000003.10:g.125939286G>A	NCBI36
NG_017037.1:g.12384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232607.7:c.492G>A MANE Select	ENSP00000232607.2:p.Gln164=
ENST00000232607.6:c.492G>A	ENSP00000232607.2:p.Gln164=
ENST00000460034.5:c.*236G>A	ENSP00000420409.1:n.*236G>A
ENST00000462091.5:c.*164G>A	ENSP00000417893.1:n.*164G>A
ENST00000467167.5:c.*390G>A	ENSP00000419618.1:n.*390G>A
ENST00000474588.5:c.311-166G>A	ENSP00000420348.1:n.311-166G>A
ENST00000479719.5:c.492G>A	ENSP00000420754.1:p.Gln164=
ENST00000497791.5:c.*164G>A	ENSP00000419121.1:n.*164G>A
ENST00000498715.1:n.210G>A
NM_000373.3:c.492G>A	NP_000364.1:p.Gln164=
NR_033434.1:n.444G>A
NR_033437.1:n.697G>A
XR_001740253.2:n.522G>A
NM_000373.4:c.492G>A MANE Select	NP_000364.1:p.Gln164=
NR_033434.2:n.358G>A
NR_033437.2:n.611G>A