Canonical Allele Identifier: CA552194401

Gene: UGT2B10

Linked Data

• gnomAD v2: 4-69682947-TCTATATCTCAGATGCAAAAATCAATAA-T
• gnomAD v3: 4-68817229-TCTATATCTCAGATGCAAAAATCAATAA-T
• gnomAD v4: 4-68817229-TCTATATCTCAGATGCAAAAATCAATAA-T
• MyVariant Identifiers: chr4:g.69682948_69682974del (hg19) ; chr4:g.68817230_68817256del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68817230_68817256del , CM000666.2:g.68817230_68817256del	GRCh38
NC_000004.11:g.69682948_69682974del , CM000666.1:g.69682948_69682974del	GRCh37
NC_000004.10:g.69717537_69717563del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265403.12:c.718+493_718+519del MANE Select	ENSP00000265403.7:n.718+493_718+519del
ENST00000265403.11:c.718+493_718+519del	ENSP00000265403.7:n.718+493_718+519del
ENST00000458688.2:c.466+745_466+771del	ENSP00000413420.2:n.466+745_466+771del
NM_001075.5:c.718+493_718+519del	NP_001066.1:n.718+493_718+519del
NM_001144767.2:c.466+745_466+771del	NP_001138239.1:n.466+745_466+771del
NM_001290091.1:c.-26-799_-26-773del	NP_001277020.1:n.-26-799_-26-773del
XM_017008585.2:c.718+493_718+519del	XP_016864074.1:n.718+493_718+519del
NM_001075.6:c.718+493_718+519del MANE Select	NP_001066.1:n.718+493_718+519del
NM_001144767.3:c.466+745_466+771del	NP_001138239.1:n.466+745_466+771del
NM_001290091.2:c.-26-799_-26-773del	NP_001277020.1:n.-26-799_-26-773del