Canonical Allele Identifier: CA1465770940

Gene: UGT2B17 UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68567372_68567373delinsTC , CM000666.2:g.68567372_68567373delinsTC	GRCh38
NC_000004.11:g.69433090_69433091delinsTC , CM000666.1:g.69433090_69433091delinsTC	GRCh37
NC_000004.10:g.69115685_69115686delinsTC	NCBI36
NG_017033.1:g.6155_6156delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.724+388_724+389delinsGA (UGT2B17) MANE Select	ENSP00000320401.2:n.724+388_724+389delinsGA
ENST00000684088.1:c.-26-1653_-26-1652delinsGA (UGT2B17)	ENSP00000507374.1:n.-26-1653_-26-1652delinsGA
ENST00000317746.2:c.724+388_724+389delinsGA (UGT2B17)	ENSP00000320401.2:n.724+388_724+389delinsGA
ENST00000616841.4:c.1733-29847_1733-29846delinsGA (UGT2B15)	ENSP00000482004.1:n.1733-29847_1733-29846delinsGA
NM_001077.3:c.724+388_724+389delinsGA (UGT2B17)	NP_001068.1:n.724+388_724+389delinsGA
XM_024454205.1:c.724+388_724+389delinsGA (UGT2B17)	XP_024309973.1:n.724+388_724+389delinsGA
NM_001077.4:c.724+388_724+389delinsGA (UGT2B17) MANE Select	NP_001068.1:n.724+388_724+389delinsGA