Canonical Allele Identifier: CA2536537026

Gene: UGT2B17 UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559926_68559927insTTTA , CM000666.2:g.68559926_68559927insTTTA	GRCh38
NC_000004.11:g.69425644_69425645insTTTA , CM000666.1:g.69425644_69425645insTTTA	GRCh37
NC_000004.10:g.69108239_69108240insTTTA	NCBI36
NG_017033.1:g.13601_13602insTAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+610_1005+611insTAAA (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+610_1005+611insTAAA
ENST00000684088.1:c.255+610_255+611insTAAA (UGT2B17)	ENSP00000507374.1:n.255+610_255+611insTAAA
ENST00000317746.2:c.1005+610_1005+611insTAAA (UGT2B17)	ENSP00000320401.2:n.1005+610_1005+611insTAAA
ENST00000616841.4:c.1733-22401_1733-22400insTAAA (UGT2B15)	ENSP00000482004.1:n.1733-22401_1733-22400insTAAA
NM_001077.3:c.1005+610_1005+611insTAAA (UGT2B17)	NP_001068.1:n.1005+610_1005+611insTAAA
XM_024454205.1:c.1005+610_1005+611insTAAA (UGT2B17)	XP_024309973.1:n.1005+610_1005+611insTAAA
NM_001077.4:c.1005+610_1005+611insTAAA (UGT2B17) MANE Select	NP_001068.1:n.1005+610_1005+611insTAAA