Canonical Allele Identifier: CA1465793615

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68669885_68669887delinsCAT , CM000666.2:g.68669885_68669887delinsCAT	GRCh38
NC_000004.11:g.69535603_69535605delinsCAT , CM000666.1:g.69535603_69535605delinsCAT	GRCh37
NC_000004.10:g.69218198_69218200delinsCAT	NCBI36
NG_052676.1:g.5890_5892delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.724+8_724+10delinsATG MANE Select	ENSP00000341045.5:n.724+8_724+10delinsATG
ENST00000338206.5:c.724+8_724+10delinsATG	ENSP00000341045.5:n.724+8_724+10delinsATG
ENST00000616841.4:c.724+8_724+10delinsATG	ENSP00000482004.1:n.724+8_724+10delinsATG
NM_001076.3:c.724+8_724+10delinsATG	NP_001067.2:n.724+8_724+10delinsATG
NM_001076.4:c.724+8_724+10delinsATG MANE Select	NP_001067.2:n.724+8_724+10delinsATG