Canonical Allele Identifier: CA2501953176

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816820_68816832del , CM000666.2:g.68816820_68816832del	GRCh38
NC_000004.11:g.69682538_69682550del , CM000666.1:g.69682538_69682550del	GRCh37
NC_000004.10:g.69717127_69717139del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+83_718+95del MANE Select	ENSP00000265403.7:n.718+83_718+95del
ENST00000265403.11:c.718+83_718+95del	ENSP00000265403.7:n.718+83_718+95del
ENST00000458688.2:c.466+335_466+347del	ENSP00000413420.2:n.466+335_466+347del
NM_001075.5:c.718+83_718+95del	NP_001066.1:n.718+83_718+95del
NM_001144767.2:c.466+335_466+347del	NP_001138239.1:n.466+335_466+347del
NM_001290091.1:c.-27+648_-27+660del	NP_001277020.1:n.-27+648_-27+660del
XM_017008585.2:c.718+83_718+95del	XP_016864074.1:n.718+83_718+95del
NM_001075.6:c.718+83_718+95del MANE Select	NP_001066.1:n.718+83_718+95del
NM_001144767.3:c.466+335_466+347del	NP_001138239.1:n.466+335_466+347del
NM_001290091.2:c.-27+648_-27+660del	NP_001277020.1:n.-27+648_-27+660del