Canonical Allele Identifier: CA1465820672

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646599_68646600delinsAG , CM000666.2:g.68646599_68646600delinsAG	GRCh38
NC_000004.11:g.69512317_69512318delinsAG , CM000666.1:g.69512317_69512318delinsAG	GRCh37
NC_000004.10:g.69194912_69194913delinsAG	NCBI36
NG_052676.1:g.29177_29178delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*504_*505delinsCT MANE Select	ENSP00000341045.5:n.*504_*505delinsCT
ENST00000616841.4:c.1732+365_1732+366delinsCT	ENSP00000482004.1:n.1732+365_1732+366delinsCT
NM_001076.3:c.*504_*505delinsCT	NP_001067.2:n.*504_*505delinsCT
NM_001076.4:c.*504_*505delinsCT MANE Select	NP_001067.2:n.*504_*505delinsCT