Canonical Allele Identifier: CA471795375
Gene: UROS HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.127477539C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788970C>G , CM000672.2:g.125788970C>G GRCh38
NC_000010.10:g.127477539C>G , CM000672.1:g.127477539C>G GRCh37
NC_000010.9:g.127467529C>G NCBI36
NG_011557.1:g.39299G>C
NG_011557.2:g.39299G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.696G>C ENSP00000518871.1:p.Leu232=
ENST00000368797.10:c.696G>C MANE Select ENSP00000357787.4:p.Leu232=
ENST00000465577.6:c.716G>C
ENST00000648427.1:c.*694G>C ENSP00000497909.1:n.*694G>C
ENST00000649536.1:c.696G>C ENSP00000497817.1:p.Leu232=
ENST00000650185.1:c.846G>C
ENST00000650472.1:n.3082G>C
ENST00000650524.1:c.609G>C ENSP00000498108.1:n.609G>C
ENST00000650587.1:c.777G>C ENSP00000497366.1:p.Leu259=
ENST00000368786.5:c.696G>C ENSP00000357775.1:p.Leu232=
ENST00000368797.8:c.696G>C ENSP00000357787.4:p.Leu232=
ENST00000464267.1:n.793G>C
ENST00000465577.5:n.338G>C
ENST00000470483.1:n.384G>C
ENST00000484541.5:n.469G>C
ENST00000616800.4:c.161-3710G>C
ENST00000622016.4:c.241-3131G>C ENSP00000483041.1:n.241-3131G>C
NM_000375.2:c.696G>C NP_000366.1:p.Leu232=
XM_005270137.2:c.777G>C XP_005270194.1:p.Leu259=
XM_005270138.2:c.696G>C XP_005270195.1:p.Leu232=
XM_005270139.2:c.661-3131G>C XP_005270196.1:n.661-3131G>C
XM_006717960.2:c.777G>C XP_006718023.1:p.Leu259=
XM_011540127.1:c.661-3710G>C XP_011538429.1:n.661-3710G>C
XR_246103.2:n.876G>C
XR_945810.1:n.1106G>C
NM_000375.3:c.696G>C MANE Select NP_000366.1:p.Leu232=
NM_001324036.1:c.777G>C NP_001310965.1:p.Leu259=
NM_001324037.1:c.696G>C NP_001310966.1:p.Leu232=
NM_001324038.1:c.615G>C NP_001310967.1:p.Leu205=
NR_136675.1:n.781G>C
NR_136676.1:n.1208G>C
NR_136677.1:n.927-3131G>C
NR_136678.1:n.692G>C
XM_011540127.2:c.661-3710G>C XP_011538429.1:n.661-3710G>C
XM_017016611.2:c.777G>C XP_016872100.2:p.Leu259=
XM_017016612.2:c.661-3131G>C XP_016872101.1:n.661-3131G>C
XM_024448154.1:c.696G>C XP_024303922.1:p.Leu232=
XR_002957010.1:n.2035G>C
XR_246103.3:n.891G>C
XR_945810.2:n.1121G>C
NM_001324036.2:c.777G>C NP_001310965.1:p.Leu259=
NM_001324037.2:c.696G>C NP_001310966.1:p.Leu232=
NM_001324038.2:c.615G>C NP_001310967.1:p.Leu205=
NR_136675.2:n.771G>C
NR_136676.2:n.1198G>C
NR_136678.2:n.682G>C
NR_136677.2:n.917-3131G>C