Canonical Allele Identifier: CA2830536973

Gene: UGT2B11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.69208629_69208630insAAAAAA , CM000666.2:g.69208629_69208630insAAAAAA	GRCh38
NC_000004.11:g.70074347_70074348insAAAAAA , CM000666.1:g.70074347_70074348insAAAAAA	GRCh37
NC_000004.10:g.70108936_70108937insAAAAAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446444.2:c.871-148_871-147insTTTTTT MANE Select	ENSP00000387683.1:n.871-148_871-147insTTTTTT
ENST00000446444.1:c.871-148_871-147insTTTTTT	ENSP00000387683.1:n.871-148_871-147insTTTTTT
ENST00000615638.4:c.871-148_871-147insTTTTTT	ENSP00000477842.1:n.871-148_871-147insTTTTTT
ENST00000620779.4:c.871-148_871-147insTTTTTT	ENSP00000478182.1:n.871-148_871-147insTTTTTT
NM_001073.1:c.871-148_871-147insTTTTTT	NP_001064.1:n.871-148_871-147insTTTTTT
XM_011531550.1:c.619-148_619-147insTTTTTT	XP_011529852.1:n.619-148_619-147insTTTTTT
XM_011531551.1:c.199-148_199-147insTTTTTT	XP_011529853.1:n.199-148_199-147insTTTTTT
NM_001073.2:c.871-148_871-147insTTTTTT	NP_001064.1:n.871-148_871-147insTTTTTT
NR_136191.1:n.598-2437_598-2436insAAAAAA
XM_011531550.2:c.619-148_619-147insTTTTTT	XP_011529852.1:n.619-148_619-147insTTTTTT
XM_017007660.2:c.124-148_124-147insTTTTTT	XP_016863149.1:n.124-148_124-147insTTTTTT
NM_001073.3:c.871-148_871-147insTTTTTT MANE Select	NP_001064.1:n.871-148_871-147insTTTTTT