Canonical Allele Identifier: CA378685921
Gene: UROS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125789004A>C , CM000672.2:g.125789004A>C GRCh38
NC_000010.10:g.127477573A>C , CM000672.1:g.127477573A>C GRCh37
NC_000010.9:g.127467563A>C NCBI36
NG_011557.1:g.39265T>G
NG_011557.2:g.39265T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.662T>G ENSP00000518871.1:p.Phe221Cys
ENST00000368797.10:c.662T>G MANE Select ENSP00000357787.4:p.Phe221Cys
ENST00000465577.6:c.682T>G
ENST00000648427.1:c.*660T>G ENSP00000497909.1:n.*660T>G
ENST00000649536.1:c.662T>G ENSP00000497817.1:p.Phe221Cys
ENST00000650185.1:c.812T>G
ENST00000650472.1:n.3048T>G
ENST00000650524.1:c.575T>G ENSP00000498108.1:n.575T>G
ENST00000650587.1:c.743T>G ENSP00000497366.1:p.Phe248Cys
ENST00000368786.5:c.662T>G ENSP00000357775.1:p.Phe221Cys
ENST00000368797.8:c.662T>G ENSP00000357787.4:p.Phe221Cys
ENST00000464267.1:n.759T>G
ENST00000465577.5:n.304T>G
ENST00000470483.1:n.350T>G
ENST00000484541.5:n.435T>G
ENST00000616800.4:c.161-3744T>G
ENST00000622016.4:c.241-3165T>G ENSP00000483041.1:n.241-3165T>G
NM_000375.2:c.662T>G NP_000366.1:p.Phe221Cys
XM_005270137.2:c.743T>G XP_005270194.1:p.Phe248Cys
XM_005270138.2:c.662T>G XP_005270195.1:p.Phe221Cys
XM_005270139.2:c.661-3165T>G XP_005270196.1:n.661-3165T>G
XM_006717960.2:c.743T>G XP_006718023.1:p.Phe248Cys
XM_011540127.1:c.661-3744T>G XP_011538429.1:n.661-3744T>G
XR_246103.2:n.842T>G
XR_945810.1:n.1072T>G
NM_000375.3:c.662T>G MANE Select NP_000366.1:p.Phe221Cys
NM_001324036.1:c.743T>G NP_001310965.1:p.Phe248Cys
NM_001324037.1:c.662T>G NP_001310966.1:p.Phe221Cys
NM_001324038.1:c.581T>G NP_001310967.1:p.Phe194Cys
NR_136675.1:n.747T>G
NR_136676.1:n.1174T>G
NR_136677.1:n.927-3165T>G
NR_136678.1:n.658T>G
XM_011540127.2:c.661-3744T>G XP_011538429.1:n.661-3744T>G
XM_017016611.2:c.743T>G XP_016872100.2:p.Phe248Cys
XM_017016612.2:c.661-3165T>G XP_016872101.1:n.661-3165T>G
XM_024448154.1:c.662T>G XP_024303922.1:p.Phe221Cys
XR_002957010.1:n.2001T>G
XR_246103.3:n.857T>G
XR_945810.2:n.1087T>G
NM_001324036.2:c.743T>G NP_001310965.1:p.Phe248Cys
NM_001324037.2:c.662T>G NP_001310966.1:p.Phe221Cys
NM_001324038.2:c.581T>G NP_001310967.1:p.Phe194Cys
NR_136675.2:n.737T>G
NR_136676.2:n.1164T>G
NR_136678.2:n.648T>G
NR_136677.2:n.917-3165T>G