Canonical Allele Identifier: CA1465760844

Gene: UGT2B17 UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559859_68559860delinsTC , CM000666.2:g.68559859_68559860delinsTC	GRCh38
NC_000004.11:g.69425577_69425578delinsTC , CM000666.1:g.69425577_69425578delinsTC	GRCh37
NC_000004.10:g.69108172_69108173delinsTC	NCBI36
NG_017033.1:g.13668_13669delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+677_1005+678delinsGA (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+677_1005+678delinsGA
ENST00000684088.1:c.255+677_255+678delinsGA (UGT2B17)	ENSP00000507374.1:n.255+677_255+678delinsGA
ENST00000317746.2:c.1005+677_1005+678delinsGA (UGT2B17)	ENSP00000320401.2:n.1005+677_1005+678delinsGA
ENST00000616841.4:c.1733-22334_1733-22333delinsGA (UGT2B15)	ENSP00000482004.1:n.1733-22334_1733-22333delinsGA
NM_001077.3:c.1005+677_1005+678delinsGA (UGT2B17)	NP_001068.1:n.1005+677_1005+678delinsGA
XM_024454205.1:c.1005+677_1005+678delinsGA (UGT2B17)	XP_024309973.1:n.1005+677_1005+678delinsGA
NM_001077.4:c.1005+677_1005+678delinsGA (UGT2B17) MANE Select	NP_001068.1:n.1005+677_1005+678delinsGA