Canonical Allele Identifier: CA1465820693

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646628_68646629delinsCT , CM000666.2:g.68646628_68646629delinsCT	GRCh38
NC_000004.11:g.69512346_69512347delinsCT , CM000666.1:g.69512346_69512347delinsCT	GRCh37
NC_000004.10:g.69194941_69194942delinsCT	NCBI36
NG_052676.1:g.29148_29149delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*475_*476delinsAG MANE Select	ENSP00000341045.5:n.*475_*476delinsAG
ENST00000616841.4:c.1732+336_1732+337delinsAG	ENSP00000482004.1:n.1732+336_1732+337delinsAG
NM_001076.3:c.*475_*476delinsAG	NP_001067.2:n.*475_*476delinsAG
NM_001076.4:c.*475_*476delinsAG MANE Select	NP_001067.2:n.*475_*476delinsAG