Canonical Allele Identifier: CA1943014059
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125823237G= , CM000672.2:g.125823237G= GRCh38
NC_000010.10:g.127511806G= , CM000672.1:g.127511806G= GRCh37
NC_000010.9:g.127501796G= NCBI36
NG_011557.1:g.5032C=
NG_029095.1:g.4703G=
NG_011557.2:g.5032C=

Transcript Alleles

HGVS Amino-acid change
ENST00000713579.1:c.-235C= ENSP00000518871.1:n.-235C=
ENST00000368797.10:c.-235C= MANE Select ENSP00000357787.4:n.-235C=
ENST00000420761.5:c.-235C= ENSP00000414833.1:n.-235C=
NM_000375.2:c.-235C= NP_000366.1:n.-235C=
XM_006717960.2:c.-57C= XP_006718023.1:n.-57C=
NM_000375.3:c.-235C= MANE Select NP_000366.1:n.-235C=
NM_001324036.1:c.-235C= NP_001310965.1:n.-235C=
NM_001324037.1:c.-235C= NP_001310966.1:n.-235C=
NM_001324038.1:c.-235C= NP_001310967.1:n.-235C=
NM_001324039.1:c.-235C= NP_001310968.1:n.-235C=
NR_136675.1:n.32C=
NR_136676.1:n.32C=
NR_136677.1:n.32C=
NR_136678.1:n.32C=
XM_017016611.2:c.-57C= XP_016872100.2:n.-57C=
XM_024448154.1:c.-57C= XP_024303922.1:n.-57C=
XM_024448155.1:c.-235C= XP_024303923.1:n.-235C=
XR_002957010.1:n.8C=
NM_001324036.2:c.-235C= NP_001310965.1:n.-235C=
NM_001324037.2:c.-235C= NP_001310966.1:n.-235C=
NM_001324038.2:c.-235C= NP_001310967.1:n.-235C=
NR_136675.2:n.22C=
NR_136676.2:n.22C=
NR_136678.2:n.22C=
NM_001324039.2:c.-235C= NP_001310968.1:n.-235C=
NR_136677.2:n.22C=