Canonical Allele Identifier: CA1943004036
Gene: UROS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125794983G= , CM000672.2:g.125794983G= GRCh38
NC_000010.10:g.127483552G= , CM000672.1:g.127483552G= GRCh37
NC_000010.9:g.127473542G= NCBI36
NG_011557.1:g.33286C=
NG_011557.2:g.33286C=

Transcript Alleles

HGVS Amino-acid change
ENST00000713579.1:c.562-5C= ENSP00000518871.1:n.562-5C=
ENST00000368797.10:c.562-5C= MANE Select ENSP00000357787.4:n.562-5C=
ENST00000465577.6:c.336-5C=
ENST00000648119.1:c.*151-5C= ENSP00000497494.1:n.*151-5C=
ENST00000648427.1:c.*314-5C= ENSP00000497909.1:n.*314-5C=
ENST00000649275.1:c.577-5C=
ENST00000649536.1:c.481-5C= ENSP00000497817.1:n.481-5C=
ENST00000650185.1:c.345-5C=
ENST00000650472.1:n.2948-5C=
ENST00000650524.1:c.475-5C= ENSP00000498108.1:n.475-5C=
ENST00000650587.1:c.562-5C= ENSP00000497366.1:n.562-5C=
ENST00000368786.5:c.562-5C= ENSP00000357775.1:n.562-5C=
ENST00000368797.8:c.562-5C= ENSP00000357787.4:n.562-5C=
ENST00000420761.5:c.478-5C= ENSP00000414833.1:n.478-5C=
ENST00000462490.5:c.221-5C=
ENST00000464267.1:n.126-5C=
ENST00000465577.5:n.123-5C=
ENST00000470483.1:n.245C=
ENST00000484541.5:n.89-5C=
ENST00000616800.4:c.62-5C=
ENST00000622016.4:c.142-5C= ENSP00000483041.1:n.142-5C=
NM_000375.2:c.562-5C= NP_000366.1:n.562-5C=
XM_005270137.2:c.562-5C= XP_005270194.1:n.562-5C=
XM_005270138.2:c.481-5C= XP_005270195.1:n.481-5C=
XM_005270139.2:c.562-5C= XP_005270196.1:n.562-5C=
XM_005270140.3:c.562-5C= XP_005270197.1:n.562-5C=
XM_006717960.2:c.562-5C= XP_006718023.1:n.562-5C=
XM_011540126.1:c.562-5C= XP_011538428.1:n.562-5C=
XM_011540127.1:c.562-5C= XP_011538429.1:n.562-5C=
XR_246103.2:n.742-5C=
XR_945809.1:n.670-5C=
XR_945810.1:n.972-5C=
NM_000375.3:c.562-5C= MANE Select NP_000366.1:n.562-5C=
NM_001324036.1:c.562-5C= NP_001310965.1:n.562-5C=
NM_001324037.1:c.481-5C= NP_001310966.1:n.481-5C=
NM_001324038.1:c.481-5C= NP_001310967.1:n.481-5C=
NR_136675.1:n.647-5C=
NR_136676.1:n.828-5C=
NR_136677.1:n.828-5C=
NR_136678.1:n.558-5C=
XM_005270140.5:c.562-5C= XP_005270197.1:n.562-5C=
XM_011540127.2:c.562-5C= XP_011538429.1:n.562-5C=
XM_017016611.2:c.562-5C= XP_016872100.2:n.562-5C=
XM_017016612.2:c.562-5C= XP_016872101.1:n.562-5C=
XM_024448154.1:c.562-5C= XP_024303922.1:n.562-5C=
XM_024448155.1:c.481-5C= XP_024303923.1:n.481-5C=
XR_001747196.2:n.685-5C=
XR_001747197.2:n.757-5C=
XR_002957009.1:n.685-5C=
XR_002957010.1:n.1901-5C=
XR_246103.3:n.757-5C=
XR_945810.2:n.987-5C=
NM_001324036.2:c.562-5C= NP_001310965.1:n.562-5C=
NM_001324037.2:c.481-5C= NP_001310966.1:n.481-5C=
NM_001324038.2:c.481-5C= NP_001310967.1:n.481-5C=
NR_136675.2:n.637-5C=
NR_136676.2:n.818-5C=
NR_136678.2:n.548-5C=
NR_136677.2:n.818-5C=