Canonical Allele Identifier: CA2670847345

Gene: UGT2B10

Linked Data

• gnomAD v4: 4-68816753-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68816754_68816755del , CM000666.2:g.68816754_68816755del	GRCh38
NC_000004.11:g.69682472_69682473del , CM000666.1:g.69682472_69682473del	GRCh37
NC_000004.10:g.69717061_69717062del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+17_718+18del MANE Select	ENSP00000265403.7:n.718+17_718+18del
ENST00000265403.11:c.718+17_718+18del	ENSP00000265403.7:n.718+17_718+18del
ENST00000458688.2:c.466+269_466+270del	ENSP00000413420.2:n.466+269_466+270del
NM_001075.5:c.718+17_718+18del	NP_001066.1:n.718+17_718+18del
NM_001144767.2:c.466+269_466+270del	NP_001138239.1:n.466+269_466+270del
NM_001290091.1:c.-27+582_-27+583del	NP_001277020.1:n.-27+582_-27+583del
XM_017008585.2:c.718+17_718+18del	XP_016864074.1:n.718+17_718+18del
NM_001075.6:c.718+17_718+18del MANE Select	NP_001066.1:n.718+17_718+18del
NM_001144767.3:c.466+269_466+270del	NP_001138239.1:n.466+269_466+270del
NM_001290091.2:c.-27+582_-27+583del	NP_001277020.1:n.-27+582_-27+583del