Canonical Allele Identifier: CA1486646065
Gene: UGT8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.114623628T= , CM000666.2:g.114623628T= GRCh38
NC_000004.11:g.115544784T= , CM000666.1:g.115544784T= GRCh37
NC_000004.10:g.115764233T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310836.11:c.748T= MANE Select ENSP00000311648.6:p.Phe250=
ENST00000310836.10:c.748T= ENSP00000311648.6:p.Phe250=
ENST00000394511.3:c.748T= ENSP00000378019.3:p.Phe250=
NM_001128174.1:c.748T= NP_001121646.1:p.Phe250=
NM_003360.3:c.748T= NP_003351.2:p.Phe250=
XM_006714302.2:c.748T= XP_006714365.1:p.Phe250=
XM_006714303.2:c.748T= XP_006714366.1:p.Phe250=
XM_011532232.1:c.748T= XP_011530534.1:p.Phe250=
NM_001128174.2:c.748T= NP_001121646.1:p.Phe250=
NM_001322112.1:c.748T= NP_001309041.1:p.Phe250=
NM_001322113.1:c.748T= NP_001309042.1:p.Phe250=
NM_001322114.1:c.748T= NP_001309043.1:p.Phe250=
NM_003360.4:c.748T= NP_003351.2:p.Phe250=
XM_024454207.1:c.748T= XP_024309975.1:p.Phe250=
XM_024454208.1:c.748T= XP_024309976.1:p.Phe250=
XM_024454209.1:c.748T= XP_024309977.1:p.Phe250=
XM_024454210.1:c.748T= XP_024309978.1:p.Phe250=
XM_024454211.1:c.748T= XP_024309979.1:p.Phe250=
NM_001128174.3:c.748T= MANE Select NP_001121646.2:p.Phe250=
NM_001322114.2:c.748T= NP_001309043.2:p.Phe250=
NM_003360.5:c.748T= NP_003351.3:p.Phe250=
NM_001322112.2:c.748T= NP_001309041.2:p.Phe250=
NM_001322113.2:c.748T= NP_001309042.2:p.Phe250=