Canonical Allele Identifier: CA1465883741

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816809_68816817delinsCCATAAAGT , CM000666.2:g.68816809_68816817delinsCCATAAAGT	GRCh38
NC_000004.11:g.69682527_69682535delinsCCATAAAGT , CM000666.1:g.69682527_69682535delinsCCATAAAGT	GRCh37
NC_000004.10:g.69717116_69717124delinsCCATAAAGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+72_718+80delinsCCATAAAGT MANE Select	ENSP00000265403.7:n.718+72_718+80delinsCCATAAAGT
ENST00000265403.11:c.718+72_718+80delinsCCATAAAGT	ENSP00000265403.7:n.718+72_718+80delinsCCATAAAGT
ENST00000458688.2:c.466+324_466+332delinsCCATAAAGT	ENSP00000413420.2:n.466+324_466+332delinsCCATAAAGT
NM_001075.5:c.718+72_718+80delinsCCATAAAGT	NP_001066.1:n.718+72_718+80delinsCCATAAAGT
NM_001144767.2:c.466+324_466+332delinsCCATAAAGT	NP_001138239.1:n.466+324_466+332delinsCCATAAAGT
NM_001290091.1:c.-27+637_-27+645delinsCCATAAAGT	NP_001277020.1:n.-27+637_-27+645delinsCCATAAAGT
XM_017008585.2:c.718+72_718+80delinsCCATAAAGT	XP_016864074.1:n.718+72_718+80delinsCCATAAAGT
NM_001075.6:c.718+72_718+80delinsCCATAAAGT MANE Select	NP_001066.1:n.718+72_718+80delinsCCATAAAGT
NM_001144767.3:c.466+324_466+332delinsCCATAAAGT	NP_001138239.1:n.466+324_466+332delinsCCATAAAGT
NM_001290091.2:c.-27+637_-27+645delinsCCATAAAGT	NP_001277020.1:n.-27+637_-27+645delinsCCATAAAGT