Canonical Allele Identifier: CA1465884043

Gene: UGT2B10

Linked Data

• dbSNP Id: rs1645084625

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817265del , CM000666.2:g.68817265del	GRCh38
NC_000004.11:g.69682983del , CM000666.1:g.69682983del	GRCh37
NC_000004.10:g.69717572del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+528del MANE Select	ENSP00000265403.7:n.718+528del
ENST00000265403.11:c.718+528del	ENSP00000265403.7:n.718+528del
ENST00000458688.2:c.467-764del	ENSP00000413420.2:n.467-764del
NM_001075.5:c.718+528del	NP_001066.1:n.718+528del
NM_001144767.2:c.467-764del	NP_001138239.1:n.467-764del
NM_001290091.1:c.-26-764del	NP_001277020.1:n.-26-764del
XM_017008585.2:c.718+528del	XP_016864074.1:n.718+528del
NM_001075.6:c.718+528del MANE Select	NP_001066.1:n.718+528del
NM_001144767.3:c.467-764del	NP_001138239.1:n.467-764del
NM_001290091.2:c.-26-764del	NP_001277020.1:n.-26-764del