Canonical Allele Identifier: CA2670847369

Gene: UGT2B10

Linked Data

• gnomAD v4: 4-68816792-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816792_68816793insA , CM000666.2:g.68816792_68816793insA	GRCh38
NC_000004.11:g.69682510_69682511insA , CM000666.1:g.69682510_69682511insA	GRCh37
NC_000004.10:g.69717099_69717100insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+55_718+56insA MANE Select	ENSP00000265403.7:n.718+55_718+56insA
ENST00000265403.11:c.718+55_718+56insA	ENSP00000265403.7:n.718+55_718+56insA
ENST00000458688.2:c.466+307_466+308insA	ENSP00000413420.2:n.466+307_466+308insA
NM_001075.5:c.718+55_718+56insA	NP_001066.1:n.718+55_718+56insA
NM_001144767.2:c.466+307_466+308insA	NP_001138239.1:n.466+307_466+308insA
NM_001290091.1:c.-27+620_-27+621insA	NP_001277020.1:n.-27+620_-27+621insA
XM_017008585.2:c.718+55_718+56insA	XP_016864074.1:n.718+55_718+56insA
NM_001075.6:c.718+55_718+56insA MANE Select	NP_001066.1:n.718+55_718+56insA
NM_001144767.3:c.466+307_466+308insA	NP_001138239.1:n.466+307_466+308insA
NM_001290091.2:c.-27+620_-27+621insA	NP_001277020.1:n.-27+620_-27+621insA