Canonical Allele Identifier: CA1465793543

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669817_68669823delinsATTATAT , CM000666.2:g.68669817_68669823delinsATTATAT	GRCh38
NC_000004.11:g.69535535_69535541delinsATTATAT , CM000666.1:g.69535535_69535541delinsATTATAT	GRCh37
NC_000004.10:g.69218130_69218136delinsATTATAT	NCBI36
NG_052676.1:g.5954_5960delinsATATAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+72_724+78delinsATATAAT MANE Select	ENSP00000341045.5:n.724+72_724+78delinsATATAAT
ENST00000338206.5:c.724+72_724+78delinsATATAAT	ENSP00000341045.5:n.724+72_724+78delinsATATAAT
ENST00000616841.4:c.724+72_724+78delinsATATAAT	ENSP00000482004.1:n.724+72_724+78delinsATATAAT
NM_001076.3:c.724+72_724+78delinsATATAAT	NP_001067.2:n.724+72_724+78delinsATATAAT
NM_001076.4:c.724+72_724+78delinsATATAAT MANE Select	NP_001067.2:n.724+72_724+78delinsATATAAT