Canonical Allele Identifier: CA1465884042

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817262_68817263delinsAT , CM000666.2:g.68817262_68817263delinsAT	GRCh38
NC_000004.11:g.69682980_69682981delinsAT , CM000666.1:g.69682980_69682981delinsAT	GRCh37
NC_000004.10:g.69717569_69717570delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+525_718+526delinsAT MANE Select	ENSP00000265403.7:n.718+525_718+526delinsAT
ENST00000265403.11:c.718+525_718+526delinsAT	ENSP00000265403.7:n.718+525_718+526delinsAT
ENST00000458688.2:c.467-767_467-766delinsAT	ENSP00000413420.2:n.467-767_467-766delinsAT
NM_001075.5:c.718+525_718+526delinsAT	NP_001066.1:n.718+525_718+526delinsAT
NM_001144767.2:c.467-767_467-766delinsAT	NP_001138239.1:n.467-767_467-766delinsAT
NM_001290091.1:c.-26-767_-26-766delinsAT	NP_001277020.1:n.-26-767_-26-766delinsAT
XM_017008585.2:c.718+525_718+526delinsAT	XP_016864074.1:n.718+525_718+526delinsAT
NM_001075.6:c.718+525_718+526delinsAT MANE Select	NP_001066.1:n.718+525_718+526delinsAT
NM_001144767.3:c.467-767_467-766delinsAT	NP_001138239.1:n.467-767_467-766delinsAT
NM_001290091.2:c.-26-767_-26-766delinsAT	NP_001277020.1:n.-26-767_-26-766delinsAT