Canonical Allele Identifier: CA435434610

Gene: UMPS

Linked Data

• MyVariant Identifiers: chr3:g.124456599G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737752G>C , CM000665.2:g.124737752G>C	GRCh38
NC_000003.11:g.124456599G>C , CM000665.1:g.124456599G>C	GRCh37
NC_000003.10:g.125939289G>C	NCBI36
NG_017037.1:g.12387G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232607.7:c.495G>C MANE Select	ENSP00000232607.2:p.Ala165=
ENST00000232607.6:c.495G>C	ENSP00000232607.2:p.Ala165=
ENST00000460034.5:c.*239G>C	ENSP00000420409.1:n.*239G>C
ENST00000462091.5:c.*167G>C	ENSP00000417893.1:n.*167G>C
ENST00000467167.5:c.*393G>C	ENSP00000419618.1:n.*393G>C
ENST00000474588.5:c.311-163G>C	ENSP00000420348.1:n.311-163G>C
ENST00000479719.5:c.495G>C	ENSP00000420754.1:p.Ala165=
ENST00000497791.5:c.*167G>C	ENSP00000419121.1:n.*167G>C
ENST00000498715.1:n.213G>C
NM_000373.3:c.495G>C	NP_000364.1:p.Ala165=
NR_033434.1:n.447G>C
NR_033437.1:n.700G>C
XR_001740253.2:n.525G>C
NM_000373.4:c.495G>C MANE Select	NP_000364.1:p.Ala165=
NR_033434.2:n.361G>C
NR_033437.2:n.614G>C