Canonical Allele Identifier: CA338748141

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404498A>T (hg19) ; chr1:g.19078004A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078004A>T , CM000663.2:g.19078004A>T	GRCh38
NC_000001.10:g.19404498A>T , CM000663.1:g.19404498A>T	GRCh37
NC_000001.9:g.19277085A>T	NCBI36
NG_027669.1:g.137249T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15296T>A MANE Select	ENSP00000364403.3:p.Leu5099His
ENST00000375224.1:c.2417T>A	ENSP00000364372.1:p.Leu806His
ENST00000375225.7:c.521T>A	ENSP00000364373.3:p.Leu174His
ENST00000375254.7:c.15296T>A	ENSP00000364403.3:p.Leu5099His
ENST00000459947.5:n.3303T>A
NM_020765.2:c.15296T>A	NP_065816.2:p.Leu5099His
XM_011541108.1:c.15449T>A	XP_011539410.1:p.Leu5150His
XM_011541109.1:c.15446T>A	XP_011539411.1:p.Leu5149His
XM_011541110.1:c.15446T>A	XP_011539412.1:p.Leu5149His
XM_011541111.1:c.15446T>A	XP_011539413.1:p.Leu5149His
XM_011541112.1:c.15434T>A	XP_011539414.1:p.Leu5145His
XM_011541113.1:c.15431T>A	XP_011539415.1:p.Leu5144His
XM_011541114.1:c.15431T>A	XP_011539416.1:p.Leu5144His
XM_011541115.1:c.15425T>A	XP_011539417.1:p.Leu5142His
XM_011541116.1:c.15416T>A	XP_011539418.1:p.Leu5139His
XM_011541117.1:c.15365T>A	XP_011539419.1:p.Leu5122His
XM_011541118.1:c.15362T>A	XP_011539420.1:p.Leu5121His
XM_011541119.1:c.15329T>A	XP_011539421.1:p.Leu5110His
XM_011541120.1:c.15326T>A	XP_011539422.1:p.Leu5109His
XM_011541121.1:c.15293T>A	XP_011539423.1:p.Leu5098His
XM_011541108.3:c.15563T>A	XP_011539410.2:p.Leu5188His
XM_011541109.3:c.15560T>A	XP_011539411.2:p.Leu5187His
XM_011541110.3:c.15560T>A	XP_011539412.2:p.Leu5187His
XM_011541111.3:c.15560T>A	XP_011539413.2:p.Leu5187His
XM_011541112.3:c.15548T>A	XP_011539414.2:p.Leu5183His
XM_011541113.3:c.15545T>A	XP_011539415.2:p.Leu5182His
XM_011541114.3:c.15545T>A	XP_011539416.2:p.Leu5182His
XM_011541115.3:c.15539T>A	XP_011539417.2:p.Leu5180His
XM_011541116.3:c.15530T>A	XP_011539418.2:p.Leu5177His
XM_011541117.3:c.15479T>A	XP_011539419.2:p.Leu5160His
XM_011541118.3:c.15476T>A	XP_011539420.2:p.Leu5159His
XM_011541119.3:c.15443T>A	XP_011539421.2:p.Leu5148His
XM_011541120.3:c.15440T>A	XP_011539422.2:p.Leu5147His
XM_011541121.3:c.15407T>A	XP_011539423.2:p.Leu5136His
XM_017000822.2:c.15542T>A	XP_016856311.2:p.Leu5181His
XM_017000823.2:c.15515T>A	XP_016856312.2:p.Leu5172His
XM_017000824.2:c.15461T>A	XP_016856313.2:p.Leu5154His
XM_017000825.2:c.15446T>A	XP_016856314.2:p.Leu5149His
XM_017000826.2:c.15443T>A	XP_016856315.2:p.Leu5148His
XM_017000827.2:c.15428T>A	XP_016856316.2:p.Leu5143His
XM_017000828.2:c.15404T>A	XP_016856317.2:p.Leu5135His
XM_017000829.2:c.15356T>A	XP_016856318.2:p.Leu5119His
XM_017000830.2:c.15305T>A	XP_016856319.2:p.Leu5102His
NM_020765.3:c.15296T>A MANE Select	NP_065816.2:p.Leu5099His