Canonical Allele Identifier: CA552177768

Gene: UGT2B15

Linked Data

• gnomAD v2: 4-69512461-C-CTTTTTTTTTTTTTTTTTTTT
• gnomAD v3: 4-68646743-C-CTTTTTTTTTTTTTTTTTTTT
• gnomAD v4: 4-68646743-C-CTTTTTTTTTTTTTTTTTTTT
• MyVariant Identifiers: chr4:g.69512461_69512462insTTTTTTTTTTTTTTTTTTTT (hg19) ; chr4:g.68646743_68646744insTTTTTTTTTTTTTTTTTTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646750_68646751insTTTTTTTTTTTTTTTTTTTT , CM000666.2:g.68646750_68646751insTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000004.11:g.69512468_69512469insTTTTTTTTTTTTTTTTTTTT , CM000666.1:g.69512468_69512469insTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000004.10:g.69195063_69195064insTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_052676.1:g.29033_29034insAAAAAAAAAAAAAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*360_*361insAAAAAAAAAAAAAAAAAAAA MANE Select	ENSP00000341045.5:n.*360_*361insAAAAAAAAAAAAAAAAAAAA
ENST00000338206.5:c.*360_*361insAAAAAAAAAAAAAAAAAAAA	ENSP00000341045.5:n.*360_*361insAAAAAAAAAAAAAAAAAAAA
ENST00000616841.4:c.1732+221_1732+222insAAAAAAAAAAAAAAAAAAAA	ENSP00000482004.1:n.1732+221_1732+222insAAAAAAAAAAAAAAAAAAAA
NM_001076.3:c.*360_*361insAAAAAAAAAAAAAAAAAAAA	NP_001067.2:n.*360_*361insAAAAAAAAAAAAAAAAAAAA
NM_001076.4:c.*360_*361insAAAAAAAAAAAAAAAAAAAA MANE Select	NP_001067.2:n.*360_*361insAAAAAAAAAAAAAAAAAAAA