Canonical Allele Identifier: CA1465820906

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646954_68646955delinsTC , CM000666.2:g.68646954_68646955delinsTC	GRCh38
NC_000004.11:g.69512672_69512673delinsTC , CM000666.1:g.69512672_69512673delinsTC	GRCh37
NC_000004.10:g.69195267_69195268delinsTC	NCBI36
NG_052676.1:g.28822_28823delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*149_*150delinsGA MANE Select	ENSP00000341045.5:n.*149_*150delinsGA
ENST00000338206.5:c.*149_*150delinsGA	ENSP00000341045.5:n.*149_*150delinsGA
ENST00000616841.4:c.1732+10_1732+11delinsGA	ENSP00000482004.1:n.1732+10_1732+11delinsGA
NM_001076.3:c.*149_*150delinsGA	NP_001067.2:n.*149_*150delinsGA
NM_001076.4:c.*149_*150delinsGA MANE Select	NP_001067.2:n.*149_*150delinsGA