Canonical Allele Identifier: CA2670847363

Gene: UGT2B10

Linked Data

• gnomAD v4: 4-68816785-CTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816786_68816788del , CM000666.2:g.68816786_68816788del	GRCh38
NC_000004.11:g.69682504_69682506del , CM000666.1:g.69682504_69682506del	GRCh37
NC_000004.10:g.69717093_69717095del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+49_718+51del MANE Select	ENSP00000265403.7:n.718+49_718+51del
ENST00000265403.11:c.718+49_718+51del	ENSP00000265403.7:n.718+49_718+51del
ENST00000458688.2:c.466+301_466+303del	ENSP00000413420.2:n.466+301_466+303del
NM_001075.5:c.718+49_718+51del	NP_001066.1:n.718+49_718+51del
NM_001144767.2:c.466+301_466+303del	NP_001138239.1:n.466+301_466+303del
NM_001290091.1:c.-27+614_-27+616del	NP_001277020.1:n.-27+614_-27+616del
XM_017008585.2:c.718+49_718+51del	XP_016864074.1:n.718+49_718+51del
NM_001075.6:c.718+49_718+51del MANE Select	NP_001066.1:n.718+49_718+51del
NM_001144767.3:c.466+301_466+303del	NP_001138239.1:n.466+301_466+303del
NM_001290091.2:c.-27+614_-27+616del	NP_001277020.1:n.-27+614_-27+616del