Canonical Allele Identifier: CA2559818015

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816944_68816945insT , CM000666.2:g.68816944_68816945insT	GRCh38
NC_000004.11:g.69682662_69682663insT , CM000666.1:g.69682662_69682663insT	GRCh37
NC_000004.10:g.69717251_69717252insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+207_718+208insT MANE Select	ENSP00000265403.7:n.718+207_718+208insT
ENST00000265403.11:c.718+207_718+208insT	ENSP00000265403.7:n.718+207_718+208insT
ENST00000458688.2:c.466+459_466+460insT	ENSP00000413420.2:n.466+459_466+460insT
NM_001075.5:c.718+207_718+208insT	NP_001066.1:n.718+207_718+208insT
NM_001144767.2:c.466+459_466+460insT	NP_001138239.1:n.466+459_466+460insT
NM_001290091.1:c.-27+772_-27+773insT	NP_001277020.1:n.-27+772_-27+773insT
XM_017008585.2:c.718+207_718+208insT	XP_016864074.1:n.718+207_718+208insT
NM_001075.6:c.718+207_718+208insT MANE Select	NP_001066.1:n.718+207_718+208insT
NM_001144767.3:c.466+459_466+460insT	NP_001138239.1:n.466+459_466+460insT
NM_001290091.2:c.-27+772_-27+773insT	NP_001277020.1:n.-27+772_-27+773insT