Canonical Allele Identifier: CA1465820866

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646884_68646885delinsTC , CM000666.2:g.68646884_68646885delinsTC	GRCh38
NC_000004.11:g.69512602_69512603delinsTC , CM000666.1:g.69512602_69512603delinsTC	GRCh37
NC_000004.10:g.69195197_69195198delinsTC	NCBI36
NG_052676.1:g.28892_28893delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*219_*220delinsGA MANE Select	ENSP00000341045.5:n.*219_*220delinsGA
ENST00000338206.5:c.*219_*220delinsGA	ENSP00000341045.5:n.*219_*220delinsGA
ENST00000616841.4:c.1732+80_1732+81delinsGA	ENSP00000482004.1:n.1732+80_1732+81delinsGA
NM_001076.3:c.*219_*220delinsGA	NP_001067.2:n.*219_*220delinsGA
NM_001076.4:c.*219_*220delinsGA MANE Select	NP_001067.2:n.*219_*220delinsGA