Canonical Allele Identifier: CA1465793532

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669807_68669809delinsATC , CM000666.2:g.68669807_68669809delinsATC	GRCh38
NC_000004.11:g.69535525_69535527delinsATC , CM000666.1:g.69535525_69535527delinsATC	GRCh37
NC_000004.10:g.69218120_69218122delinsATC	NCBI36
NG_052676.1:g.5968_5970delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+86_724+88delinsGAT MANE Select	ENSP00000341045.5:n.724+86_724+88delinsGAT
ENST00000338206.5:c.724+86_724+88delinsGAT	ENSP00000341045.5:n.724+86_724+88delinsGAT
ENST00000616841.4:c.724+86_724+88delinsGAT	ENSP00000482004.1:n.724+86_724+88delinsGAT
NM_001076.3:c.724+86_724+88delinsGAT	NP_001067.2:n.724+86_724+88delinsGAT
NM_001076.4:c.724+86_724+88delinsGAT MANE Select	NP_001067.2:n.724+86_724+88delinsGAT