Canonical Allele Identifier: CA1465820756

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646728_68646729delinsTA , CM000666.2:g.68646728_68646729delinsTA	GRCh38
NC_000004.11:g.69512446_69512447delinsTA , CM000666.1:g.69512446_69512447delinsTA	GRCh37
NC_000004.10:g.69195041_69195042delinsTA	NCBI36
NG_052676.1:g.29048_29049delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*375_*376delinsTA MANE Select	ENSP00000341045.5:n.*375_*376delinsTA
ENST00000338206.5:c.*375_*376delinsTA	ENSP00000341045.5:n.*375_*376delinsTA
ENST00000616841.4:c.1732+236_1732+237delinsTA	ENSP00000482004.1:n.1732+236_1732+237delinsTA
NM_001076.3:c.*375_*376delinsTA	NP_001067.2:n.*375_*376delinsTA
NM_001076.4:c.*375_*376delinsTA MANE Select	NP_001067.2:n.*375_*376delinsTA