Canonical Allele Identifier: CA1465770971

Gene: UGT2B17 UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68567417_68567418delinsTG , CM000666.2:g.68567417_68567418delinsTG	GRCh38
NC_000004.11:g.69433135_69433136delinsTG , CM000666.1:g.69433135_69433136delinsTG	GRCh37
NC_000004.10:g.69115730_69115731delinsTG	NCBI36
NG_017033.1:g.6110_6111delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.724+343_724+344delinsCA (UGT2B17) MANE Select	ENSP00000320401.2:n.724+343_724+344delinsCA
ENST00000684088.1:c.-26-1698_-26-1697delinsCA (UGT2B17)	ENSP00000507374.1:n.-26-1698_-26-1697delinsCA
ENST00000317746.2:c.724+343_724+344delinsCA (UGT2B17)	ENSP00000320401.2:n.724+343_724+344delinsCA
ENST00000616841.4:c.1733-29892_1733-29891delinsCA (UGT2B15)	ENSP00000482004.1:n.1733-29892_1733-29891delinsCA
NM_001077.3:c.724+343_724+344delinsCA (UGT2B17)	NP_001068.1:n.724+343_724+344delinsCA
XM_024454205.1:c.724+343_724+344delinsCA (UGT2B17)	XP_024309973.1:n.724+343_724+344delinsCA
NM_001077.4:c.724+343_724+344delinsCA (UGT2B17) MANE Select	NP_001068.1:n.724+343_724+344delinsCA