Canonical Allele Identifier: CA1465820682

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646610_68646611delinsTA , CM000666.2:g.68646610_68646611delinsTA	GRCh38
NC_000004.11:g.69512328_69512329delinsTA , CM000666.1:g.69512328_69512329delinsTA	GRCh37
NC_000004.10:g.69194923_69194924delinsTA	NCBI36
NG_052676.1:g.29166_29167delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*493_*494delinsTA MANE Select	ENSP00000341045.5:n.*493_*494delinsTA
ENST00000616841.4:c.1732+354_1732+355delinsTA	ENSP00000482004.1:n.1732+354_1732+355delinsTA
NM_001076.3:c.*493_*494delinsTA	NP_001067.2:n.*493_*494delinsTA
NM_001076.4:c.*493_*494delinsTA MANE Select	NP_001067.2:n.*493_*494delinsTA