Canonical Allele Identifier: CA1465760773
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68559779_68559786delinsCTGATTCT , CM000666.2:g.68559779_68559786delinsCTGATTCT GRCh38
NC_000004.11:g.69425497_69425504delinsCTGATTCT , CM000666.1:g.69425497_69425504delinsCTGATTCT GRCh37
NC_000004.10:g.69108092_69108099delinsCTGATTCT NCBI36
NG_017033.1:g.13742_13749delinsAGAATCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000317746.3:c.1005+751_1005+758delinsAGAATCAG (UGT2B17) MANE Select ENSP00000320401.2:n.1005+751_1005+758delinsAGAATCAG
ENST00000684088.1:c.255+751_255+758delinsAGAATCAG (UGT2B17) ENSP00000507374.1:n.255+751_255+758delinsAGAATCAG
ENST00000317746.2:c.1005+751_1005+758delinsAGAATCAG (UGT2B17) ENSP00000320401.2:n.1005+751_1005+758delinsAGAATCAG
ENST00000616841.4:c.1733-22260_1733-22253delinsAGAATCAG (UGT2B15) ENSP00000482004.1:n.1733-22260_1733-22253delinsAGAATCAG
NM_001077.3:c.1005+751_1005+758delinsAGAATCAG (UGT2B17) NP_001068.1:n.1005+751_1005+758delinsAGAATCAG
XM_024454205.1:c.1005+751_1005+758delinsAGAATCAG (UGT2B17) XP_024309973.1:n.1005+751_1005+758delinsAGAATCAG
NM_001077.4:c.1005+751_1005+758delinsAGAATCAG (UGT2B17) MANE Select NP_001068.1:n.1005+751_1005+758delinsAGAATCAG