Canonical Allele Identifier: CA471795317
Gene: UROS HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.127477470G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788901G>A , CM000672.2:g.125788901G>A GRCh38
NC_000010.10:g.127477470G>A , CM000672.1:g.127477470G>A GRCh37
NC_000010.9:g.127467460G>A NCBI36
NG_011557.1:g.39368C>T
NG_011557.2:g.39368C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000713579.1:c.765C>T ENSP00000518871.1:p.Ile255=
ENST00000368797.10:c.765C>T MANE Select ENSP00000357787.4:p.Ile255=
ENST00000465577.6:c.785C>T
ENST00000648427.1:c.*763C>T ENSP00000497909.1:n.*763C>T
ENST00000649536.1:c.765C>T ENSP00000497817.1:p.Ile255=
ENST00000650472.1:n.3151C>T
ENST00000650524.1:c.678C>T ENSP00000498108.1:n.678C>T
ENST00000650587.1:c.846C>T ENSP00000497366.1:p.Ile282=
ENST00000368786.5:c.765C>T ENSP00000357775.1:p.Ile255=
ENST00000368797.8:c.765C>T ENSP00000357787.4:p.Ile255=
ENST00000464267.1:n.862C>T
ENST00000465577.5:n.407C>T
ENST00000470483.1:n.453C>T
ENST00000484541.5:n.538C>T
ENST00000616800.4:c.161-3641C>T
ENST00000622016.4:c.241-3062C>T ENSP00000483041.1:n.241-3062C>T
NM_000375.2:c.765C>T NP_000366.1:p.Ile255=
XM_005270137.2:c.846C>T XP_005270194.1:p.Ile282=
XM_005270138.2:c.765C>T XP_005270195.1:p.Ile255=
XM_005270139.2:c.661-3062C>T XP_005270196.1:n.661-3062C>T
XM_006717960.2:c.846C>T XP_006718023.1:p.Ile282=
XM_011540127.1:c.661-3641C>T XP_011538429.1:n.661-3641C>T
XR_246103.2:n.945C>T
XR_945810.1:n.1175C>T
NM_000375.3:c.765C>T MANE Select NP_000366.1:p.Ile255=
NM_001324036.1:c.846C>T NP_001310965.1:p.Ile282=
NM_001324037.1:c.765C>T NP_001310966.1:p.Ile255=
NM_001324038.1:c.684C>T NP_001310967.1:p.Ile228=
NR_136675.1:n.850C>T
NR_136676.1:n.1277C>T
NR_136677.1:n.927-3062C>T
NR_136678.1:n.761C>T
XM_011540127.2:c.661-3641C>T XP_011538429.1:n.661-3641C>T
XM_017016611.2:c.846C>T XP_016872100.2:p.Ile282=
XM_017016612.2:c.661-3062C>T XP_016872101.1:n.661-3062C>T
XM_024448154.1:c.765C>T XP_024303922.1:p.Ile255=
XR_002957010.1:n.2104C>T
XR_246103.3:n.960C>T
XR_945810.2:n.1190C>T
NM_001324036.2:c.846C>T NP_001310965.1:p.Ile282=
NM_001324037.2:c.765C>T NP_001310966.1:p.Ile255=
NM_001324038.2:c.684C>T NP_001310967.1:p.Ile228=
NR_136675.2:n.840C>T
NR_136676.2:n.1267C>T
NR_136678.2:n.751C>T
NR_136677.2:n.917-3062C>T