Canonical Allele Identifier: CA1063752499

Gene: UGT2B15

Linked Data

• dbSNP Id: rs4148274
• gnomAD v3: 4-68646729-A-ATTTTTTTTTTTTTTTTTTTTTTTTATTCCTGGTTTAAAAAAAAGAGTTTTTTT
• gnomAD v4: 4-68646729-A-ATTTTTTTTTTTTTTTTTTTTTTTTATTCCTGGTTTAAAAAAAAGAGTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646741_68646742insTTTTTTTTTTTTATTCCTGGTTTAAAAAAAAGAGTTTTTTTTTTTTTTTTTTT , CM000666.2:g.68646741_68646742insTTTTTTTTTTTTATTCCTGGTTTAAAAAAAAGAGTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000004.11:g.69512459_69512460insTTTTTTTTTTTTATTCCTGGTTTAAAAAAAAGAGTTTTTTTTTTTTTTTTTTT , CM000666.1:g.69512459_69512460insTTTTTTTTTTTTATTCCTGGTTTAAAAAAAAGAGTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000004.10:g.69195054_69195055insTTTTTTTTTTTTATTCCTGGTTTAAAAAAAAGAGTTTTTTTTTTTTTTTTTTT	NCBI36
NG_052676.1:g.29047_29048insAAAAAAACTCTTTTTTTTAAACCAGGAATAAAAAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*374_*375insAAAAAAACTCTTTTTTTTAAACCAGGAATAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	ENSP00000341045.5:n.*374_*375insAAAAAAACTCTTTTTTTTAAACCAGGAAT...
ENST00000338206.5:c.*374_*375insAAAAAAACTCTTTTTTTTAAACCAGGAATAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000341045.5:n.*374_*375insAAAAAAACTCTTTTTTTTAAACCAGGAAT...
ENST00000616841.4:c.1732+235_1732+236insAAAAAAACTCTTTTTTTTAAACCAGGAATAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000482004.1:n.1732+235_1732+236insAAAAAAACTCTTTTTTTTAAA...
NM_001076.3:c.*374_*375insAAAAAAACTCTTTTTTTTAAACCAGGAATAAAAAAAAAAAAAAAAAAAAAAAA	NP_001067.2:n.*374_*375insAAAAAAACTCTTTTTTTTAAACCAGGAATAAAAAA...
NM_001076.4:c.*374_*375insAAAAAAACTCTTTTTTTTAAACCAGGAATAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	NP_001067.2:n.*374_*375insAAAAAAACTCTTTTTTTTAAACCAGGAATAAAAAA...