Canonical Allele Identifier: CA2542451659

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817154_68817155del , CM000666.2:g.68817154_68817155del	GRCh38
NC_000004.11:g.69682872_69682873del , CM000666.1:g.69682872_69682873del	GRCh37
NC_000004.10:g.69717461_69717462del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+417_718+418del MANE Select	ENSP00000265403.7:n.718+417_718+418del
ENST00000265403.11:c.718+417_718+418del	ENSP00000265403.7:n.718+417_718+418del
ENST00000458688.2:c.466+669_466+670del	ENSP00000413420.2:n.466+669_466+670del
NM_001075.5:c.718+417_718+418del	NP_001066.1:n.718+417_718+418del
NM_001144767.2:c.466+669_466+670del	NP_001138239.1:n.466+669_466+670del
NM_001290091.1:c.-26-875_-26-874del	NP_001277020.1:n.-26-875_-26-874del
XM_017008585.2:c.718+417_718+418del	XP_016864074.1:n.718+417_718+418del
NM_001075.6:c.718+417_718+418del MANE Select	NP_001066.1:n.718+417_718+418del
NM_001144767.3:c.466+669_466+670del	NP_001138239.1:n.466+669_466+670del
NM_001290091.2:c.-26-875_-26-874del	NP_001277020.1:n.-26-875_-26-874del