Canonical Allele Identifier: CA1465761022

Gene: UGT2B17 UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559991_68559995delinsATTCT , CM000666.2:g.68559991_68559995delinsATTCT	GRCh38
NC_000004.11:g.69425709_69425713delinsATTCT , CM000666.1:g.69425709_69425713delinsATTCT	GRCh37
NC_000004.10:g.69108304_69108308delinsATTCT	NCBI36
NG_017033.1:g.13533_13537delinsAGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+542_1005+546delinsAGAAT (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+542_1005+546delinsAGAAT
ENST00000684088.1:c.255+542_255+546delinsAGAAT (UGT2B17)	ENSP00000507374.1:n.255+542_255+546delinsAGAAT
ENST00000317746.2:c.1005+542_1005+546delinsAGAAT (UGT2B17)	ENSP00000320401.2:n.1005+542_1005+546delinsAGAAT
ENST00000616841.4:c.1733-22469_1733-22465delinsAGAAT (UGT2B15)	ENSP00000482004.1:n.1733-22469_1733-22465delinsAGAAT
NM_001077.3:c.1005+542_1005+546delinsAGAAT (UGT2B17)	NP_001068.1:n.1005+542_1005+546delinsAGAAT
XM_024454205.1:c.1005+542_1005+546delinsAGAAT (UGT2B17)	XP_024309973.1:n.1005+542_1005+546delinsAGAAT
NM_001077.4:c.1005+542_1005+546delinsAGAAT (UGT2B17) MANE Select	NP_001068.1:n.1005+542_1005+546delinsAGAAT