Canonical Allele Identifier: CA1943013971
Gene: UROS HGNC NCBI

Linked Data

dbSNP Id: rs1854152860

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125823147del , CM000672.2:g.125823147del GRCh38
NC_000010.10:g.127511716del , CM000672.1:g.127511716del GRCh37
NC_000010.9:g.127501706del NCBI36
NG_011557.1:g.5126del
NG_029095.1:g.4613del
NG_011557.2:g.5126del

Transcript Alleles

HGVS Amino-acid change
ENST00000713579.1:c.-141del ENSP00000518871.1:n.-141del
ENST00000368797.10:c.-141del MANE Select ENSP00000357787.4:n.-141del
ENST00000648119.1:c.-141del ENSP00000497494.1:n.-141del
ENST00000648427.1:c.-141del ENSP00000497909.1:n.-141del
ENST00000649536.1:c.-141del ENSP00000497817.1:n.-141del
ENST00000368778.7:c.-141del ENSP00000357767.3:n.-141del
ENST00000368797.8:c.-141del ENSP00000357787.4:n.-141del
ENST00000420761.5:c.-141del ENSP00000414833.1:n.-141del
NM_000375.2:c.-141del NP_000366.1:n.-141del
XM_006717960.2:c.-27+64del XP_006718023.1:n.-27+64del
NM_000375.3:c.-141del MANE Select NP_000366.1:n.-141del
NM_001324036.1:c.-141del NP_001310965.1:n.-141del
NM_001324037.1:c.-141del NP_001310966.1:n.-141del
NM_001324038.1:c.-141del NP_001310967.1:n.-141del
NM_001324039.1:c.-141del NP_001310968.1:n.-141del
NR_136675.1:n.126del
NR_136676.1:n.126del
NR_136677.1:n.126del
NR_136678.1:n.126del
XM_017016611.2:c.-27+64del XP_016872100.2:n.-27+64del
XM_024448154.1:c.-27+64del XP_024303922.1:n.-27+64del
XM_024448155.1:c.-141del XP_024303923.1:n.-141del
XR_002957010.1:n.38+64del
NM_001324036.2:c.-141del NP_001310965.1:n.-141del
NM_001324037.2:c.-141del NP_001310966.1:n.-141del
NM_001324038.2:c.-141del NP_001310967.1:n.-141del
NR_136675.2:n.116del
NR_136676.2:n.116del
NR_136678.2:n.116del
NM_001324039.2:c.-141del NP_001310968.1:n.-141del
NR_136677.2:n.116del