Canonical Allele Identifier: CA354275565

Gene: UMPS

Linked Data

• dbSNP Id: rs2150896729
• MyVariant Identifiers: chr3:g.124456738A>T (hg19) ; chr3:g.124737891A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.124737891A>T , CM000665.2:g.124737891A>T	GRCh38
NC_000003.11:g.124456738A>T , CM000665.1:g.124456738A>T	GRCh37
NC_000003.10:g.125939428A>T	NCBI36
NG_017037.1:g.12526A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000232607.7:c.634A>T MANE Select	ENSP00000232607.2:p.Asn212Tyr
ENST00000232607.6:c.634A>T	ENSP00000232607.2:p.Asn212Tyr
ENST00000460034.5:c.*378A>T	ENSP00000420409.1:n.*378A>T
ENST00000462091.5:c.*306A>T	ENSP00000417893.1:n.*306A>T
ENST00000467167.5:c.*532A>T	ENSP00000419618.1:n.*532A>T
ENST00000474588.5:c.311-24A>T	ENSP00000420348.1:n.311-24A>T
ENST00000479719.5:c.634A>T	ENSP00000420754.1:p.Asn212Tyr
ENST00000497791.5:c.*306A>T	ENSP00000419121.1:n.*306A>T
ENST00000498715.1:n.352A>T
NM_000373.3:c.634A>T	NP_000364.1:p.Asn212Tyr
NR_033434.1:n.586A>T
NR_033437.1:n.839A>T
XR_001740253.2:n.664A>T
NM_000373.4:c.634A>T MANE Select	NP_000364.1:p.Asn212Tyr
NR_033434.2:n.500A>T
NR_033437.2:n.753A>T