Canonical Allele Identifier: CA1465820757

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646729_68646731delinsATT , CM000666.2:g.68646729_68646731delinsATT	GRCh38
NC_000004.11:g.69512447_69512449delinsATT , CM000666.1:g.69512447_69512449delinsATT	GRCh37
NC_000004.10:g.69195042_69195044delinsATT	NCBI36
NG_052676.1:g.29046_29048delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*373_*375delinsAAT MANE Select	ENSP00000341045.5:n.*373_*375delinsAAT
ENST00000338206.5:c.*373_*375delinsAAT	ENSP00000341045.5:n.*373_*375delinsAAT
ENST00000616841.4:c.1732+234_1732+236delinsAAT	ENSP00000482004.1:n.1732+234_1732+236delinsAAT
NM_001076.3:c.*373_*375delinsAAT	NP_001067.2:n.*373_*375delinsAAT
NM_001076.4:c.*373_*375delinsAAT MANE Select	NP_001067.2:n.*373_*375delinsAAT