Canonical Allele Identifier: CA2611361960
Gene: UROS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.125788673_125788674insGGTTTA , CM000672.2:g.125788673_125788674insGGTTTA GRCh38
NC_000010.10:g.127477242_127477243insGGTTTA , CM000672.1:g.127477242_127477243insGGTTTA GRCh37
NC_000010.9:g.127467232_127467233insGGTTTA NCBI36
NG_011557.1:g.39595_39596insTAAACC
NG_011557.2:g.39595_39596insTAAACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000713579.1:c.*194_*195insTAAACC ENSP00000518871.1:n.*194_*195insTAAACC
ENST00000368797.10:c.*194_*195insTAAACC MANE Select ENSP00000357787.4:n.*194_*195insTAAACC
ENST00000465577.6:c.1012_1013insTAAACC
ENST00000648427.1:c.*990_*991insTAAACC ENSP00000497909.1:n.*990_*991insTAAACC
ENST00000649536.1:c.*194_*195insTAAACC ENSP00000497817.1:n.*194_*195insTAAACC
ENST00000650472.1:n.3378_3379insTAAACC
ENST00000650524.1:c.905_906insTAAACC ENSP00000498108.1:n.905_906insTAAACC
ENST00000650587.1:c.*194_*195insTAAACC ENSP00000497366.1:n.*194_*195insTAAACC
ENST00000368786.5:c.*194_*195insTAAACC ENSP00000357775.1:n.*194_*195insTAAACC
ENST00000368797.8:c.*194_*195insTAAACC ENSP00000357787.4:n.*194_*195insTAAACC
ENST00000465577.5:n.634_635insTAAACC
ENST00000470483.1:n.680_681insTAAACC
ENST00000484541.5:n.765_766insTAAACC
ENST00000616800.4:c.161-3414_161-3413insTAAACC
ENST00000622016.4:c.241-2835_241-2834insTAAACC ENSP00000483041.1:n.241-2835_241-2834insTAAACC
NM_000375.2:c.*194_*195insTAAACC NP_000366.1:n.*194_*195insTAAACC
XM_005270137.2:c.*194_*195insTAAACC XP_005270194.1:n.*194_*195insTAAACC
XM_005270138.2:c.*194_*195insTAAACC XP_005270195.1:n.*194_*195insTAAACC
XM_005270139.2:c.661-2835_661-2834insTAAACC XP_005270196.1:n.661-2835_661-2834insTAAACC
XM_006717960.2:c.*194_*195insTAAACC XP_006718023.1:n.*194_*195insTAAACC
XM_011540127.1:c.661-3414_661-3413insTAAACC XP_011538429.1:n.661-3414_661-3413insTAAACC
XR_246103.2:n.1172_1173insTAAACC
XR_945810.1:n.1402_1403insTAAACC
NM_000375.3:c.*194_*195insTAAACC MANE Select NP_000366.1:n.*194_*195insTAAACC
NM_001324036.1:c.*194_*195insTAAACC NP_001310965.1:n.*194_*195insTAAACC
NM_001324037.1:c.*194_*195insTAAACC NP_001310966.1:n.*194_*195insTAAACC
NM_001324038.1:c.*194_*195insTAAACC NP_001310967.1:n.*194_*195insTAAACC
NR_136675.1:n.1077_1078insTAAACC
NR_136676.1:n.1504_1505insTAAACC
NR_136677.1:n.927-2835_927-2834insTAAACC
NR_136678.1:n.988_989insTAAACC
XM_011540127.2:c.661-3414_661-3413insTAAACC XP_011538429.1:n.661-3414_661-3413insTAAACC
XM_017016611.2:c.*194_*195insTAAACC XP_016872100.2:n.*194_*195insTAAACC
XM_017016612.2:c.661-2835_661-2834insTAAACC XP_016872101.1:n.661-2835_661-2834insTAAACC
XM_024448154.1:c.*194_*195insTAAACC XP_024303922.1:n.*194_*195insTAAACC
XR_002957010.1:n.2331_2332insTAAACC
XR_246103.3:n.1187_1188insTAAACC
XR_945810.2:n.1417_1418insTAAACC
NM_001324036.2:c.*194_*195insTAAACC NP_001310965.1:n.*194_*195insTAAACC
NM_001324037.2:c.*194_*195insTAAACC NP_001310966.1:n.*194_*195insTAAACC
NM_001324038.2:c.*194_*195insTAAACC NP_001310967.1:n.*194_*195insTAAACC
NR_136675.2:n.1067_1068insTAAACC
NR_136676.2:n.1494_1495insTAAACC
NR_136678.2:n.978_979insTAAACC
NR_136677.2:n.917-2835_917-2834insTAAACC