Canonical Allele Identifier: CA1943009976
Gene: UROS HGNC NCBI

Linked Data

dbSNP Id: rs1853170672

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125814992T>A , CM000672.2:g.125814992T>A GRCh38
NC_000010.10:g.127503561T>A , CM000672.1:g.127503561T>A GRCh37
NC_000010.9:g.127493551T>A NCBI36
NG_011557.1:g.13277A>T
NG_011557.2:g.13277A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000713579.1:c.244+42A>T ENSP00000518871.1:n.244+42A>T
ENST00000368797.10:c.244+42A>T MANE Select ENSP00000357787.4:n.244+42A>T
ENST00000648119.1:c.244+42A>T ENSP00000497494.1:n.244+42A>T
ENST00000648427.1:c.244+42A>T ENSP00000497909.1:n.244+42A>T
ENST00000649275.1:c.173+42A>T
ENST00000649450.1:n.281+42A>T
ENST00000649536.1:c.244+42A>T ENSP00000497817.1:n.244+42A>T
ENST00000650185.1:c.27+42A>T
ENST00000650524.1:c.49+42A>T ENSP00000498108.1:n.49+42A>T
ENST00000650587.1:c.244+42A>T ENSP00000497366.1:n.244+42A>T
ENST00000368774.1:c.244+42A>T ENSP00000357763.1:n.244+42A>T
ENST00000368778.7:c.244+42A>T ENSP00000357767.3:n.244+42A>T
ENST00000368786.5:c.244+42A>T ENSP00000357775.1:n.244+42A>T
ENST00000368797.8:c.244+42A>T ENSP00000357787.4:n.244+42A>T
ENST00000420761.5:c.160+42A>T ENSP00000414833.1:n.160+42A>T
NM_000375.2:c.244+42A>T NP_000366.1:n.244+42A>T
XM_005270137.2:c.244+42A>T XP_005270194.1:n.244+42A>T
XM_005270138.2:c.244+42A>T XP_005270195.1:n.244+42A>T
XM_005270139.2:c.244+42A>T XP_005270196.1:n.244+42A>T
XM_005270140.3:c.244+42A>T XP_005270197.1:n.244+42A>T
XM_005270141.1:c.244+42A>T XP_005270198.1:n.244+42A>T
XM_006717960.2:c.244+42A>T XP_006718023.1:n.244+42A>T
XM_011540126.1:c.244+42A>T XP_011538428.1:n.244+42A>T
XM_011540127.1:c.244+42A>T XP_011538429.1:n.244+42A>T
XR_246103.2:n.352+42A>T
XR_945809.1:n.352+42A>T
XR_945810.1:n.352+42A>T
NM_000375.3:c.244+42A>T MANE Select NP_000366.1:n.244+42A>T
NM_001324036.1:c.244+42A>T NP_001310965.1:n.244+42A>T
NM_001324037.1:c.244+42A>T NP_001310966.1:n.244+42A>T
NM_001324038.1:c.244+42A>T NP_001310967.1:n.244+42A>T
NM_001324039.1:c.244+42A>T NP_001310968.1:n.244+42A>T
NR_136675.1:n.329+1445A>T
NR_136676.1:n.510+42A>T
NR_136677.1:n.510+42A>T
NR_136678.1:n.241-2704A>T
XM_005270140.5:c.244+42A>T XP_005270197.1:n.244+42A>T
XM_011540127.2:c.244+42A>T XP_011538429.1:n.244+42A>T
XM_017016611.2:c.244+42A>T XP_016872100.2:n.244+42A>T
XM_017016612.2:c.244+42A>T XP_016872101.1:n.244+42A>T
XM_024448154.1:c.244+42A>T XP_024303922.1:n.244+42A>T
XM_024448155.1:c.244+42A>T XP_024303923.1:n.244+42A>T
XR_001747196.2:n.367+42A>T
XR_001747197.2:n.367+42A>T
XR_002957009.1:n.367+42A>T
XR_002957010.1:n.308+42A>T
XR_246103.3:n.367+42A>T
XR_945810.2:n.367+42A>T
NM_001324036.2:c.244+42A>T NP_001310965.1:n.244+42A>T
NM_001324037.2:c.244+42A>T NP_001310966.1:n.244+42A>T
NM_001324038.2:c.244+42A>T NP_001310967.1:n.244+42A>T
NR_136675.2:n.319+1445A>T
NR_136676.2:n.500+42A>T
NR_136678.2:n.231-2704A>T
NM_001324039.2:c.244+42A>T NP_001310968.1:n.244+42A>T
NR_136677.2:n.500+42A>T