Canonical Allele Identifier: CA1465820667

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646597_68646598delinsTA , CM000666.2:g.68646597_68646598delinsTA	GRCh38
NC_000004.11:g.69512315_69512316delinsTA , CM000666.1:g.69512315_69512316delinsTA	GRCh37
NC_000004.10:g.69194910_69194911delinsTA	NCBI36
NG_052676.1:g.29179_29180delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*506_*507delinsTA MANE Select	ENSP00000341045.5:n.*506_*507delinsTA
ENST00000616841.4:c.1732+367_1732+368delinsTA	ENSP00000482004.1:n.1732+367_1732+368delinsTA
NM_001076.3:c.*506_*507delinsTA	NP_001067.2:n.*506_*507delinsTA
NM_001076.4:c.*506_*507delinsTA MANE Select	NP_001067.2:n.*506_*507delinsTA