Canonical Allele Identifier: CA1398971032

Gene: UMPS

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737589G= , CM000665.2:g.124737589G=	GRCh38
NC_000003.11:g.124456436G= , CM000665.1:g.124456436G=	GRCh37
NC_000003.10:g.125939126G=	NCBI36
NG_017037.1:g.12224G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000232607.7:c.332G= MANE Select	ENSP00000232607.2:p.Gly111=
ENST00000232607.6:c.332G=	ENSP00000232607.2:p.Gly111=
ENST00000460034.5:c.*76G=	ENSP00000420409.1:n.*76G=
ENST00000462091.5:c.*4G=	ENSP00000417893.1:n.*4G=
ENST00000467167.5:c.*230G=	ENSP00000419618.1:n.*230G=
ENST00000474588.5:c.311-326G=	ENSP00000420348.1:n.311-326G=
ENST00000479719.5:c.332G=	ENSP00000420754.1:p.Gly111=
ENST00000497791.5:c.*4G=	ENSP00000419121.1:n.*4G=
ENST00000498715.1:n.50G=
NM_000373.3:c.332G=	NP_000364.1:p.Gly111=
NR_033434.1:n.284G=
NR_033437.1:n.537G=
XR_001740253.2:n.362G=
NM_000373.4:c.332G= MANE Select	NP_000364.1:p.Gly111=
NR_033434.2:n.198G=
NR_033437.2:n.451G=