Canonical Allele Identifier: CA1465883722
Gene: UGT2B10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68816770_68816771delinsCT , CM000666.2:g.68816770_68816771delinsCT GRCh38
NC_000004.11:g.69682488_69682489delinsCT , CM000666.1:g.69682488_69682489delinsCT GRCh37
NC_000004.10:g.69717077_69717078delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265403.12:c.718+33_718+34delinsCT MANE Select ENSP00000265403.7:n.718+33_718+34delinsCT
ENST00000265403.11:c.718+33_718+34delinsCT ENSP00000265403.7:n.718+33_718+34delinsCT
ENST00000458688.2:c.466+285_466+286delinsCT ENSP00000413420.2:n.466+285_466+286delinsCT
NM_001075.5:c.718+33_718+34delinsCT NP_001066.1:n.718+33_718+34delinsCT
NM_001144767.2:c.466+285_466+286delinsCT NP_001138239.1:n.466+285_466+286delinsCT
NM_001290091.1:c.-27+598_-27+599delinsCT NP_001277020.1:n.-27+598_-27+599delinsCT
XM_017008585.2:c.718+33_718+34delinsCT XP_016864074.1:n.718+33_718+34delinsCT
NM_001075.6:c.718+33_718+34delinsCT MANE Select NP_001066.1:n.718+33_718+34delinsCT
NM_001144767.3:c.466+285_466+286delinsCT NP_001138239.1:n.466+285_466+286delinsCT
NM_001290091.2:c.-27+598_-27+599delinsCT NP_001277020.1:n.-27+598_-27+599delinsCT