Canonical Allele Identifier: CA2473585855
Gene: UROD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45015395_45015403delinsTTGCCAACC , CM000663.2:g.45015395_45015403delinsTTGCCAACC GRCh38
NC_000001.10:g.45481067_45481075delinsTTGCCAACC , CM000663.1:g.45481067_45481075delinsTTGCCAACC GRCh37
NC_000001.9:g.45253654_45253662delinsTTGCCAACC NCBI36
NG_007122.2:g.8238_8246delinsTTGCCAACC
NG_033058.1:g.953_961delinsGGTTGGCAA

Transcript Alleles

HGVS Amino-acid change
ENST00000246337.9:c.1001_1009delinsTTGCCAACC MANE Select ENSP00000246337.4:p.Ile334=
ENST00000491773.6:c.758_766delinsTTGCCAACC ENSP00000498551.1:p.Ile253=
ENST00000636293.1:c.863_871delinsTTGCCAACC ENSP00000490710.1:p.Ile288=
ENST00000636836.1:c.*37_*45delinsTTGCCAACC ENSP00000490594.1:n.*37_*45delinsTTGCCAAC...
ENST00000651476.1:c.896_904delinsTTGCCAACC ENSP00000498668.1:p.Ile299=
ENST00000652165.1:c.758_766delinsTTGCCAACC ENSP00000498295.1:p.Ile253=
ENST00000652287.1:c.938_946delinsTTGCCAACC ENSP00000498413.1:p.Ile313=
ENST00000652514.1:c.962_970delinsTTGCCAACC ENSP00000498635.1:n.962_970delinsTTGCCAAC...
ENST00000246337.8:c.1001_1009delinsTTGCCAACC ENSP00000246337.4:p.Ile334=
ENST00000465678.1:n.746_754delinsTTGCCAACC
ENST00000472254.1:n.754_762delinsTTGCCAACC
ENST00000494399.5:n.1668_1676delinsTTGCCAACC
NM_000374.4:c.1001_1009delinsTTGCCAACC NP_000365.3:p.Ile334=
NR_036510.1:n.1184_1192delinsTTGCCAACC
XM_005271169.1:c.785_793delinsTTGCCAACC XP_005271226.1:p.Ile262=
XM_005271170.1:c.785_793delinsTTGCCAACC XP_005271227.1:p.Ile262=
XM_011542080.1:c.938_946delinsTTGCCAACC XP_011540382.1:p.Ile313=
XM_011542081.1:c.833_841delinsTTGCCAACC XP_011540383.1:p.Ile278=
NM_000374.5:c.1001_1009delinsTTGCCAACC MANE Select NP_000365.3:p.Ile334=
NR_158184.1:n.1082_1090delinsTTGCCAACC
NR_158185.1:n.1032_1040delinsTTGCCAACC
NR_036510.2:n.1063_1071delinsTTGCCAACC