Canonical Allele Identifier: CA338748165

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15286T>C MANE Select	ENSP00000364403.3:p.Phe5096Leu
ENST00000375224.1:c.2407T>C	ENSP00000364372.1:p.Phe803Leu
ENST00000375225.7:c.511T>C	ENSP00000364373.3:p.Phe171Leu
ENST00000375254.7:c.15286T>C	ENSP00000364403.3:p.Phe5096Leu
ENST00000459947.5:n.3293T>C
NM_020765.2:c.15286T>C	NP_065816.2:p.Phe5096Leu
XM_011541108.1:c.15439T>C	XP_011539410.1:p.Phe5147Leu
XM_011541109.1:c.15436T>C	XP_011539411.1:p.Phe5146Leu
XM_011541110.1:c.15436T>C	XP_011539412.1:p.Phe5146Leu
XM_011541111.1:c.15436T>C	XP_011539413.1:p.Phe5146Leu
XM_011541112.1:c.15424T>C	XP_011539414.1:p.Phe5142Leu
XM_011541113.1:c.15421T>C	XP_011539415.1:p.Phe5141Leu
XM_011541114.1:c.15421T>C	XP_011539416.1:p.Phe5141Leu
XM_011541115.1:c.15415T>C	XP_011539417.1:p.Phe5139Leu
XM_011541116.1:c.15406T>C	XP_011539418.1:p.Phe5136Leu
XM_011541117.1:c.15355T>C	XP_011539419.1:p.Phe5119Leu
XM_011541118.1:c.15352T>C	XP_011539420.1:p.Phe5118Leu
XM_011541119.1:c.15319T>C	XP_011539421.1:p.Phe5107Leu
XM_011541120.1:c.15316T>C	XP_011539422.1:p.Phe5106Leu
XM_011541121.1:c.15283T>C	XP_011539423.1:p.Phe5095Leu
XM_011541108.3:c.15553T>C	XP_011539410.2:p.Phe5185Leu
XM_011541109.3:c.15550T>C	XP_011539411.2:p.Phe5184Leu
XM_011541110.3:c.15550T>C	XP_011539412.2:p.Phe5184Leu
XM_011541111.3:c.15550T>C	XP_011539413.2:p.Phe5184Leu
XM_011541112.3:c.15538T>C	XP_011539414.2:p.Phe5180Leu
XM_011541113.3:c.15535T>C	XP_011539415.2:p.Phe5179Leu
XM_011541114.3:c.15535T>C	XP_011539416.2:p.Phe5179Leu
XM_011541115.3:c.15529T>C	XP_011539417.2:p.Phe5177Leu
XM_011541116.3:c.15520T>C	XP_011539418.2:p.Phe5174Leu
XM_011541117.3:c.15469T>C	XP_011539419.2:p.Phe5157Leu
XM_011541118.3:c.15466T>C	XP_011539420.2:p.Phe5156Leu
XM_011541119.3:c.15433T>C	XP_011539421.2:p.Phe5145Leu
XM_011541120.3:c.15430T>C	XP_011539422.2:p.Phe5144Leu
XM_011541121.3:c.15397T>C	XP_011539423.2:p.Phe5133Leu
XM_017000822.2:c.15532T>C	XP_016856311.2:p.Phe5178Leu
XM_017000823.2:c.15505T>C	XP_016856312.2:p.Phe5169Leu
XM_017000824.2:c.15451T>C	XP_016856313.2:p.Phe5151Leu
XM_017000825.2:c.15436T>C	XP_016856314.2:p.Phe5146Leu
XM_017000826.2:c.15433T>C	XP_016856315.2:p.Phe5145Leu
XM_017000827.2:c.15418T>C	XP_016856316.2:p.Phe5140Leu
XM_017000828.2:c.15394T>C	XP_016856317.2:p.Phe5132Leu
XM_017000829.2:c.15346T>C	XP_016856318.2:p.Phe5116Leu
XM_017000830.2:c.15295T>C	XP_016856319.2:p.Phe5099Leu
NM_020765.3:c.15286T>C MANE Select	NP_065816.2:p.Phe5096Leu