Canonical Allele Identifier: CA354272772

Gene: UMPS

Linked Data

• MyVariant Identifiers: chr3:g.124456451G>T (hg19) ; chr3:g.124737604G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737604G>T , CM000665.2:g.124737604G>T	GRCh38
NC_000003.11:g.124456451G>T , CM000665.1:g.124456451G>T	GRCh37
NC_000003.10:g.125939141G>T	NCBI36
NG_017037.1:g.12239G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232607.7:c.347G>T MANE Select	ENSP00000232607.2:p.Gly116Val
ENST00000232607.6:c.347G>T	ENSP00000232607.2:p.Gly116Val
ENST00000460034.5:c.*91G>T	ENSP00000420409.1:n.*91G>T
ENST00000462091.5:c.*19G>T	ENSP00000417893.1:n.*19G>T
ENST00000467167.5:c.*245G>T	ENSP00000419618.1:n.*245G>T
ENST00000474588.5:c.311-311G>T	ENSP00000420348.1:n.311-311G>T
ENST00000479719.5:c.347G>T	ENSP00000420754.1:p.Gly116Val
ENST00000497791.5:c.*19G>T	ENSP00000419121.1:n.*19G>T
ENST00000498715.1:n.65G>T
NM_000373.3:c.347G>T	NP_000364.1:p.Gly116Val
NR_033434.1:n.299G>T
NR_033437.1:n.552G>T
XR_001740253.2:n.377G>T
NM_000373.4:c.347G>T MANE Select	NP_000364.1:p.Gly116Val
NR_033434.2:n.213G>T
NR_033437.2:n.466G>T