Canonical Allele Identifier: CA1465820749

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646720_68646722delinsAAG , CM000666.2:g.68646720_68646722delinsAAG	GRCh38
NC_000004.11:g.69512438_69512440delinsAAG , CM000666.1:g.69512438_69512440delinsAAG	GRCh37
NC_000004.10:g.69195033_69195035delinsAAG	NCBI36
NG_052676.1:g.29055_29057delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*382_*384delinsCTT MANE Select	ENSP00000341045.5:n.*382_*384delinsCTT
ENST00000338206.5:c.*382_*384delinsCTT	ENSP00000341045.5:n.*382_*384delinsCTT
ENST00000616841.4:c.1732+243_1732+245delinsCTT	ENSP00000482004.1:n.1732+243_1732+245delinsCTT
NM_001076.3:c.*382_*384delinsCTT	NP_001067.2:n.*382_*384delinsCTT
NM_001076.4:c.*382_*384delinsCTT MANE Select	NP_001067.2:n.*382_*384delinsCTT