Canonical Allele Identifier: CA1465820698

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646638_68646654delinsTATGGCTTGGATGACAC , CM000666.2:g.68646638_68646654delinsTATGGCTTGGATGACAC	GRCh38
NC_000004.11:g.69512356_69512372delinsTATGGCTTGGATGACAC , CM000666.1:g.69512356_69512372delinsTATGGCTTGGATGACAC	GRCh37
NC_000004.10:g.69194951_69194967delinsTATGGCTTGGATGACAC	NCBI36
NG_052676.1:g.29123_29139delinsGTGTCATCCAAGCCATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*450_*466delinsGTGTCATCCAAGCCATA MANE Select	ENSP00000341045.5:n.*450_*466delinsGTGTCATCCAAGCCATA
ENST00000338206.5:c.*450_*466delinsGTGTCATCCAAGCCATA	ENSP00000341045.5:n.*450_*466delinsGTGTCATCCAAGCCATA
ENST00000616841.4:c.1732+311_1732+327delinsGTGTCATCCAAGCCATA	ENSP00000482004.1:n.1732+311_1732+327delinsGTGTCATCCAAGCCATA
NM_001076.3:c.*450_*466delinsGTGTCATCCAAGCCATA	NP_001067.2:n.*450_*466delinsGTGTCATCCAAGCCATA
NM_001076.4:c.*450_*466delinsGTGTCATCCAAGCCATA MANE Select	NP_001067.2:n.*450_*466delinsGTGTCATCCAAGCCATA