Canonical Allele Identifier: CA338748161

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404507A>C (hg19) ; chr1:g.19078013A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078013A>C , CM000663.2:g.19078013A>C	GRCh38
NC_000001.10:g.19404507A>C , CM000663.1:g.19404507A>C	GRCh37
NC_000001.9:g.19277094A>C	NCBI36
NG_027669.1:g.137240T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15287T>G MANE Select	ENSP00000364403.3:p.Phe5096Cys
ENST00000375224.1:c.2408T>G	ENSP00000364372.1:p.Phe803Cys
ENST00000375225.7:c.512T>G	ENSP00000364373.3:p.Phe171Cys
ENST00000375254.7:c.15287T>G	ENSP00000364403.3:p.Phe5096Cys
ENST00000459947.5:n.3294T>G
NM_020765.2:c.15287T>G	NP_065816.2:p.Phe5096Cys
XM_011541108.1:c.15440T>G	XP_011539410.1:p.Phe5147Cys
XM_011541109.1:c.15437T>G	XP_011539411.1:p.Phe5146Cys
XM_011541110.1:c.15437T>G	XP_011539412.1:p.Phe5146Cys
XM_011541111.1:c.15437T>G	XP_011539413.1:p.Phe5146Cys
XM_011541112.1:c.15425T>G	XP_011539414.1:p.Phe5142Cys
XM_011541113.1:c.15422T>G	XP_011539415.1:p.Phe5141Cys
XM_011541114.1:c.15422T>G	XP_011539416.1:p.Phe5141Cys
XM_011541115.1:c.15416T>G	XP_011539417.1:p.Phe5139Cys
XM_011541116.1:c.15407T>G	XP_011539418.1:p.Phe5136Cys
XM_011541117.1:c.15356T>G	XP_011539419.1:p.Phe5119Cys
XM_011541118.1:c.15353T>G	XP_011539420.1:p.Phe5118Cys
XM_011541119.1:c.15320T>G	XP_011539421.1:p.Phe5107Cys
XM_011541120.1:c.15317T>G	XP_011539422.1:p.Phe5106Cys
XM_011541121.1:c.15284T>G	XP_011539423.1:p.Phe5095Cys
XM_011541108.3:c.15554T>G	XP_011539410.2:p.Phe5185Cys
XM_011541109.3:c.15551T>G	XP_011539411.2:p.Phe5184Cys
XM_011541110.3:c.15551T>G	XP_011539412.2:p.Phe5184Cys
XM_011541111.3:c.15551T>G	XP_011539413.2:p.Phe5184Cys
XM_011541112.3:c.15539T>G	XP_011539414.2:p.Phe5180Cys
XM_011541113.3:c.15536T>G	XP_011539415.2:p.Phe5179Cys
XM_011541114.3:c.15536T>G	XP_011539416.2:p.Phe5179Cys
XM_011541115.3:c.15530T>G	XP_011539417.2:p.Phe5177Cys
XM_011541116.3:c.15521T>G	XP_011539418.2:p.Phe5174Cys
XM_011541117.3:c.15470T>G	XP_011539419.2:p.Phe5157Cys
XM_011541118.3:c.15467T>G	XP_011539420.2:p.Phe5156Cys
XM_011541119.3:c.15434T>G	XP_011539421.2:p.Phe5145Cys
XM_011541120.3:c.15431T>G	XP_011539422.2:p.Phe5144Cys
XM_011541121.3:c.15398T>G	XP_011539423.2:p.Phe5133Cys
XM_017000822.2:c.15533T>G	XP_016856311.2:p.Phe5178Cys
XM_017000823.2:c.15506T>G	XP_016856312.2:p.Phe5169Cys
XM_017000824.2:c.15452T>G	XP_016856313.2:p.Phe5151Cys
XM_017000825.2:c.15437T>G	XP_016856314.2:p.Phe5146Cys
XM_017000826.2:c.15434T>G	XP_016856315.2:p.Phe5145Cys
XM_017000827.2:c.15419T>G	XP_016856316.2:p.Phe5140Cys
XM_017000828.2:c.15395T>G	XP_016856317.2:p.Phe5132Cys
XM_017000829.2:c.15347T>G	XP_016856318.2:p.Phe5116Cys
XM_017000830.2:c.15296T>G	XP_016856319.2:p.Phe5099Cys
NM_020765.3:c.15287T>G MANE Select	NP_065816.2:p.Phe5096Cys