Canonical Allele Identifier: CA2943279

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68830733A>G , CM000666.2:g.68830733A>G	GRCh38
NC_000004.11:g.69696451A>G , CM000666.1:g.69696451A>G	GRCh37
NC_000004.10:g.69731040A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.1441A>G MANE Select	ENSP00000265403.7:p.Asn481Asp
ENST00000265403.11:c.1441A>G	ENSP00000265403.7:p.Asn481Asp
ENST00000458688.2:c.1189A>G	ENSP00000413420.2:p.Asn397Asp
NM_001075.5:c.1441A>G	NP_001066.1:p.Asn481Asp
NM_001144767.2:c.1189A>G	NP_001138239.1:p.Asn397Asp
NM_001290091.1:c.697A>G	NP_001277020.1:p.Asn233Asp
XM_017008585.2:c.1432A>G	XP_016864074.1:p.Asn478Asp
NM_001075.6:c.1441A>G MANE Select	NP_001066.1:p.Asn481Asp
NM_001144767.3:c.1189A>G	NP_001138239.1:p.Asn397Asp
NM_001290091.2:c.697A>G	NP_001277020.1:p.Asn233Asp