Canonical Allele Identifier: CA338748166

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404508A>T (hg19) ; chr1:g.19078014A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078014A>T , CM000663.2:g.19078014A>T	GRCh38
NC_000001.10:g.19404508A>T , CM000663.1:g.19404508A>T	GRCh37
NC_000001.9:g.19277095A>T	NCBI36
NG_027669.1:g.137239T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15286T>A MANE Select	ENSP00000364403.3:p.Phe5096Ile
ENST00000375224.1:c.2407T>A	ENSP00000364372.1:p.Phe803Ile
ENST00000375225.7:c.511T>A	ENSP00000364373.3:p.Phe171Ile
ENST00000375254.7:c.15286T>A	ENSP00000364403.3:p.Phe5096Ile
ENST00000459947.5:n.3293T>A
NM_020765.2:c.15286T>A	NP_065816.2:p.Phe5096Ile
XM_011541108.1:c.15439T>A	XP_011539410.1:p.Phe5147Ile
XM_011541109.1:c.15436T>A	XP_011539411.1:p.Phe5146Ile
XM_011541110.1:c.15436T>A	XP_011539412.1:p.Phe5146Ile
XM_011541111.1:c.15436T>A	XP_011539413.1:p.Phe5146Ile
XM_011541112.1:c.15424T>A	XP_011539414.1:p.Phe5142Ile
XM_011541113.1:c.15421T>A	XP_011539415.1:p.Phe5141Ile
XM_011541114.1:c.15421T>A	XP_011539416.1:p.Phe5141Ile
XM_011541115.1:c.15415T>A	XP_011539417.1:p.Phe5139Ile
XM_011541116.1:c.15406T>A	XP_011539418.1:p.Phe5136Ile
XM_011541117.1:c.15355T>A	XP_011539419.1:p.Phe5119Ile
XM_011541118.1:c.15352T>A	XP_011539420.1:p.Phe5118Ile
XM_011541119.1:c.15319T>A	XP_011539421.1:p.Phe5107Ile
XM_011541120.1:c.15316T>A	XP_011539422.1:p.Phe5106Ile
XM_011541121.1:c.15283T>A	XP_011539423.1:p.Phe5095Ile
XM_011541108.3:c.15553T>A	XP_011539410.2:p.Phe5185Ile
XM_011541109.3:c.15550T>A	XP_011539411.2:p.Phe5184Ile
XM_011541110.3:c.15550T>A	XP_011539412.2:p.Phe5184Ile
XM_011541111.3:c.15550T>A	XP_011539413.2:p.Phe5184Ile
XM_011541112.3:c.15538T>A	XP_011539414.2:p.Phe5180Ile
XM_011541113.3:c.15535T>A	XP_011539415.2:p.Phe5179Ile
XM_011541114.3:c.15535T>A	XP_011539416.2:p.Phe5179Ile
XM_011541115.3:c.15529T>A	XP_011539417.2:p.Phe5177Ile
XM_011541116.3:c.15520T>A	XP_011539418.2:p.Phe5174Ile
XM_011541117.3:c.15469T>A	XP_011539419.2:p.Phe5157Ile
XM_011541118.3:c.15466T>A	XP_011539420.2:p.Phe5156Ile
XM_011541119.3:c.15433T>A	XP_011539421.2:p.Phe5145Ile
XM_011541120.3:c.15430T>A	XP_011539422.2:p.Phe5144Ile
XM_011541121.3:c.15397T>A	XP_011539423.2:p.Phe5133Ile
XM_017000822.2:c.15532T>A	XP_016856311.2:p.Phe5178Ile
XM_017000823.2:c.15505T>A	XP_016856312.2:p.Phe5169Ile
XM_017000824.2:c.15451T>A	XP_016856313.2:p.Phe5151Ile
XM_017000825.2:c.15436T>A	XP_016856314.2:p.Phe5146Ile
XM_017000826.2:c.15433T>A	XP_016856315.2:p.Phe5145Ile
XM_017000827.2:c.15418T>A	XP_016856316.2:p.Phe5140Ile
XM_017000828.2:c.15394T>A	XP_016856317.2:p.Phe5132Ile
XM_017000829.2:c.15346T>A	XP_016856318.2:p.Phe5116Ile
XM_017000830.2:c.15295T>A	XP_016856319.2:p.Phe5099Ile
NM_020765.3:c.15286T>A MANE Select	NP_065816.2:p.Phe5096Ile