Canonical Allele Identifier: CA1465794685
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670502_68670505delinsCATA , CM000666.2:g.68670502_68670505delinsCATA GRCh38
NC_000004.11:g.69536220_69536223delinsCATA , CM000666.1:g.69536220_69536223delinsCATA GRCh37
NC_000004.10:g.69218815_69218818delinsCATA NCBI36
NG_052676.1:g.5272_5275delinsTATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.114_117delinsTATG MANE Select ENSP00000341045.5:p.Asn38=
ENST00000338206.5:c.114_117delinsTATG ENSP00000341045.5:p.Asn38=
ENST00000616841.4:c.114_117delinsTATG ENSP00000482004.1:p.Asn38=
NM_001076.3:c.114_117delinsTATG NP_001067.2:p.Asn38=
NM_001076.4:c.114_117delinsTATG MANE Select NP_001067.2:p.Asn38=
Search 100 bp 5'
Search 100 bp 3'