Canonical Allele Identifier: CA1465760914

Gene: UGT2B17 UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559920_68559921delinsAG , CM000666.2:g.68559920_68559921delinsAG	GRCh38
NC_000004.11:g.69425638_69425639delinsAG , CM000666.1:g.69425638_69425639delinsAG	GRCh37
NC_000004.10:g.69108233_69108234delinsAG	NCBI36
NG_017033.1:g.13607_13608delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+616_1005+617delinsCT (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+616_1005+617delinsCT
ENST00000684088.1:c.255+616_255+617delinsCT (UGT2B17)	ENSP00000507374.1:n.255+616_255+617delinsCT
ENST00000317746.2:c.1005+616_1005+617delinsCT (UGT2B17)	ENSP00000320401.2:n.1005+616_1005+617delinsCT
ENST00000616841.4:c.1733-22395_1733-22394delinsCT (UGT2B15)	ENSP00000482004.1:n.1733-22395_1733-22394delinsCT
NM_001077.3:c.1005+616_1005+617delinsCT (UGT2B17)	NP_001068.1:n.1005+616_1005+617delinsCT
XM_024454205.1:c.1005+616_1005+617delinsCT (UGT2B17)	XP_024309973.1:n.1005+616_1005+617delinsCT
NM_001077.4:c.1005+616_1005+617delinsCT (UGT2B17) MANE Select	NP_001068.1:n.1005+616_1005+617delinsCT