Canonical Allele Identifier: CA1465883717

Gene: UGT2B10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816766_68816768delinsAGC , CM000666.2:g.68816766_68816768delinsAGC	GRCh38
NC_000004.11:g.69682484_69682486delinsAGC , CM000666.1:g.69682484_69682486delinsAGC	GRCh37
NC_000004.10:g.69717073_69717075delinsAGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+29_718+31delinsAGC MANE Select	ENSP00000265403.7:n.718+29_718+31delinsAGC
ENST00000265403.11:c.718+29_718+31delinsAGC	ENSP00000265403.7:n.718+29_718+31delinsAGC
ENST00000458688.2:c.466+281_466+283delinsAGC	ENSP00000413420.2:n.466+281_466+283delinsAGC
NM_001075.5:c.718+29_718+31delinsAGC	NP_001066.1:n.718+29_718+31delinsAGC
NM_001144767.2:c.466+281_466+283delinsAGC	NP_001138239.1:n.466+281_466+283delinsAGC
NM_001290091.1:c.-27+594_-27+596delinsAGC	NP_001277020.1:n.-27+594_-27+596delinsAGC
XM_017008585.2:c.718+29_718+31delinsAGC	XP_016864074.1:n.718+29_718+31delinsAGC
NM_001075.6:c.718+29_718+31delinsAGC MANE Select	NP_001066.1:n.718+29_718+31delinsAGC
NM_001144767.3:c.466+281_466+283delinsAGC	NP_001138239.1:n.466+281_466+283delinsAGC
NM_001290091.2:c.-27+594_-27+596delinsAGC	NP_001277020.1:n.-27+594_-27+596delinsAGC