Canonical Allele Identifier: CA1943010600
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125816456_125816458delinsCCA , CM000672.2:g.125816456_125816458delinsCCA GRCh38
NC_000010.10:g.127505025_127505027delinsCCA , CM000672.1:g.127505025_127505027delinsCCA GRCh37
NC_000010.9:g.127495015_127495017delinsCCA NCBI36
NG_011557.1:g.11811_11813delinsTGG
NG_011557.2:g.11811_11813delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.42_44delinsTGG ENSP00000518871.1:p.Cys14=
ENST00000368797.10:c.42_44delinsTGG MANE Select ENSP00000357787.4:p.Cys14=
ENST00000648119.1:c.42_44delinsTGG ENSP00000497494.1:p.Cys14=
ENST00000648427.1:c.42_44delinsTGG ENSP00000497909.1:p.Cys14=
ENST00000649450.1:n.79_81delinsTGG
ENST00000649536.1:c.42_44delinsTGG ENSP00000497817.1:p.Cys14=
ENST00000650587.1:c.42_44delinsTGG ENSP00000497366.1:p.Cys14=
ENST00000368774.1:c.42_44delinsTGG ENSP00000357763.1:p.Cys14=
ENST00000368778.7:c.42_44delinsTGG ENSP00000357767.3:p.Cys14=
ENST00000368786.5:c.42_44delinsTGG ENSP00000357775.1:p.Cys14=
ENST00000368797.8:c.42_44delinsTGG ENSP00000357787.4:p.Cys14=
ENST00000420761.5:c.42_44delinsTGG ENSP00000414833.1:p.Cys14=
NM_000375.2:c.42_44delinsTGG NP_000366.1:p.Cys14=
XM_005270137.2:c.42_44delinsTGG XP_005270194.1:p.Cys14=
XM_005270138.2:c.42_44delinsTGG XP_005270195.1:p.Cys14=
XM_005270139.2:c.42_44delinsTGG XP_005270196.1:p.Cys14=
XM_005270140.3:c.42_44delinsTGG XP_005270197.1:p.Cys14=
XM_005270141.1:c.42_44delinsTGG XP_005270198.1:p.Cys14=
XM_006717960.2:c.42_44delinsTGG XP_006718023.1:p.Cys14=
XM_011540126.1:c.42_44delinsTGG XP_011538428.1:p.Cys14=
XM_011540127.1:c.42_44delinsTGG XP_011538429.1:p.Cys14=
XR_246103.2:n.150_152delinsTGG
XR_945809.1:n.150_152delinsTGG
XR_945810.1:n.150_152delinsTGG
NM_000375.3:c.42_44delinsTGG MANE Select NP_000366.1:p.Cys14=
NM_001324036.1:c.42_44delinsTGG NP_001310965.1:p.Cys14=
NM_001324037.1:c.42_44delinsTGG NP_001310966.1:p.Cys14=
NM_001324038.1:c.42_44delinsTGG NP_001310967.1:p.Cys14=
NM_001324039.1:c.42_44delinsTGG NP_001310968.1:p.Cys14=
NR_136675.1:n.308_310delinsTGG
NR_136676.1:n.308_310delinsTGG
NR_136677.1:n.308_310delinsTGG
NR_136678.1:n.241-4170_241-4168delinsTGG
XM_005270140.5:c.42_44delinsTGG XP_005270197.1:p.Cys14=
XM_011540127.2:c.42_44delinsTGG XP_011538429.1:p.Cys14=
XM_017016611.2:c.42_44delinsTGG XP_016872100.2:p.Cys14=
XM_017016612.2:c.42_44delinsTGG XP_016872101.1:p.Cys14=
XM_024448154.1:c.42_44delinsTGG XP_024303922.1:p.Cys14=
XM_024448155.1:c.42_44delinsTGG XP_024303923.1:p.Cys14=
XR_001747196.2:n.165_167delinsTGG
XR_001747197.2:n.165_167delinsTGG
XR_002957009.1:n.165_167delinsTGG
XR_002957010.1:n.106_108delinsTGG
XR_246103.3:n.165_167delinsTGG
XR_945810.2:n.165_167delinsTGG
NM_001324036.2:c.42_44delinsTGG NP_001310965.1:p.Cys14=
NM_001324037.2:c.42_44delinsTGG NP_001310966.1:p.Cys14=
NM_001324038.2:c.42_44delinsTGG NP_001310967.1:p.Cys14=
NR_136675.2:n.298_300delinsTGG
NR_136676.2:n.298_300delinsTGG
NR_136678.2:n.231-4170_231-4168delinsTGG
NM_001324039.2:c.42_44delinsTGG NP_001310968.1:p.Cys14=
NR_136677.2:n.298_300delinsTGG