Canonical Allele Identifier: CA1465883730

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816785_68816786delinsCT , CM000666.2:g.68816785_68816786delinsCT	GRCh38
NC_000004.11:g.69682503_69682504delinsCT , CM000666.1:g.69682503_69682504delinsCT	GRCh37
NC_000004.10:g.69717092_69717093delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+48_718+49delinsCT MANE Select	ENSP00000265403.7:n.718+48_718+49delinsCT
ENST00000265403.11:c.718+48_718+49delinsCT	ENSP00000265403.7:n.718+48_718+49delinsCT
ENST00000458688.2:c.466+300_466+301delinsCT	ENSP00000413420.2:n.466+300_466+301delinsCT
NM_001075.5:c.718+48_718+49delinsCT	NP_001066.1:n.718+48_718+49delinsCT
NM_001144767.2:c.466+300_466+301delinsCT	NP_001138239.1:n.466+300_466+301delinsCT
NM_001290091.1:c.-27+613_-27+614delinsCT	NP_001277020.1:n.-27+613_-27+614delinsCT
XM_017008585.2:c.718+48_718+49delinsCT	XP_016864074.1:n.718+48_718+49delinsCT
NM_001075.6:c.718+48_718+49delinsCT MANE Select	NP_001066.1:n.718+48_718+49delinsCT
NM_001144767.3:c.466+300_466+301delinsCT	NP_001138239.1:n.466+300_466+301delinsCT
NM_001290091.2:c.-27+613_-27+614delinsCT	NP_001277020.1:n.-27+613_-27+614delinsCT