Canonical Allele Identifier: CA1943014061
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125823239A= , CM000672.2:g.125823239A= GRCh38
NC_000010.10:g.127511808A= , CM000672.1:g.127511808A= GRCh37
NC_000010.9:g.127501798A= NCBI36
NG_011557.1:g.5030T=
NG_029095.1:g.4705A=
NG_011557.2:g.5030T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.-237T= ENSP00000518871.1:n.-237T=
ENST00000368797.10:c.-237T= MANE Select ENSP00000357787.4:n.-237T=
ENST00000420761.5:c.-237T= ENSP00000414833.1:n.-237T=
NM_000375.2:c.-237T= NP_000366.1:n.-237T=
XM_006717960.2:c.-59T= XP_006718023.1:n.-59T=
NM_000375.3:c.-237T= MANE Select NP_000366.1:n.-237T=
NM_001324036.1:c.-237T= NP_001310965.1:n.-237T=
NM_001324037.1:c.-237T= NP_001310966.1:n.-237T=
NM_001324038.1:c.-237T= NP_001310967.1:n.-237T=
NM_001324039.1:c.-237T= NP_001310968.1:n.-237T=
NR_136675.1:n.30T=
NR_136676.1:n.30T=
NR_136677.1:n.30T=
NR_136678.1:n.30T=
XM_017016611.2:c.-59T= XP_016872100.2:n.-59T=
XM_024448154.1:c.-59T= XP_024303922.1:n.-59T=
XM_024448155.1:c.-237T= XP_024303923.1:n.-237T=
XR_002957010.1:n.6T=
NM_001324036.2:c.-237T= NP_001310965.1:n.-237T=
NM_001324037.2:c.-237T= NP_001310966.1:n.-237T=
NM_001324038.2:c.-237T= NP_001310967.1:n.-237T=
NR_136675.2:n.20T=
NR_136676.2:n.20T=
NR_136678.2:n.20T=
NM_001324039.2:c.-237T= NP_001310968.1:n.-237T=
NR_136677.2:n.20T=