Canonical Allele Identifier: CA1465820687

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646618_68646623delinsTTTTTC , CM000666.2:g.68646618_68646623delinsTTTTTC	GRCh38
NC_000004.11:g.69512336_69512341delinsTTTTTC , CM000666.1:g.69512336_69512341delinsTTTTTC	GRCh37
NC_000004.10:g.69194931_69194936delinsTTTTTC	NCBI36
NG_052676.1:g.29154_29159delinsGAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*481_*486delinsGAAAAA MANE Select	ENSP00000341045.5:n.*481_*486delinsGAAAAA
ENST00000616841.4:c.1732+342_1732+347delinsGAAAAA	ENSP00000482004.1:n.1732+342_1732+347delinsGAAAAA
NM_001076.3:c.*481_*486delinsGAAAAA	NP_001067.2:n.*481_*486delinsGAAAAA
NM_001076.4:c.*481_*486delinsGAAAAA MANE Select	NP_001067.2:n.*481_*486delinsGAAAAA