Canonical Allele Identifier: CA1465820692

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646627_68646628delinsTC , CM000666.2:g.68646627_68646628delinsTC	GRCh38
NC_000004.11:g.69512345_69512346delinsTC , CM000666.1:g.69512345_69512346delinsTC	GRCh37
NC_000004.10:g.69194940_69194941delinsTC	NCBI36
NG_052676.1:g.29149_29150delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*476_*477delinsGA MANE Select	ENSP00000341045.5:n.*476_*477delinsGA
ENST00000616841.4:c.1732+337_1732+338delinsGA	ENSP00000482004.1:n.1732+337_1732+338delinsGA
NM_001076.3:c.*476_*477delinsGA	NP_001067.2:n.*476_*477delinsGA
NM_001076.4:c.*476_*477delinsGA MANE Select	NP_001067.2:n.*476_*477delinsGA