Canonical Allele Identifier: CA338748190

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404516G>C (hg19) ; chr1:g.19078022G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078022G>C , CM000663.2:g.19078022G>C	GRCh38
NC_000001.10:g.19404516G>C , CM000663.1:g.19404516G>C	GRCh37
NC_000001.9:g.19277103G>C	NCBI36
NG_027669.1:g.137231C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15278C>G MANE Select	ENSP00000364403.3:p.Ser5093Cys
ENST00000375224.1:c.2399C>G	ENSP00000364372.1:p.Ser800Cys
ENST00000375225.7:c.503C>G	ENSP00000364373.3:p.Ser168Cys
ENST00000375254.7:c.15278C>G	ENSP00000364403.3:p.Ser5093Cys
ENST00000459947.5:n.3285C>G
NM_020765.2:c.15278C>G	NP_065816.2:p.Ser5093Cys
XM_011541108.1:c.15431C>G	XP_011539410.1:p.Ser5144Cys
XM_011541109.1:c.15428C>G	XP_011539411.1:p.Ser5143Cys
XM_011541110.1:c.15428C>G	XP_011539412.1:p.Ser5143Cys
XM_011541111.1:c.15428C>G	XP_011539413.1:p.Ser5143Cys
XM_011541112.1:c.15416C>G	XP_011539414.1:p.Ser5139Cys
XM_011541113.1:c.15413C>G	XP_011539415.1:p.Ser5138Cys
XM_011541114.1:c.15413C>G	XP_011539416.1:p.Ser5138Cys
XM_011541115.1:c.15407C>G	XP_011539417.1:p.Ser5136Cys
XM_011541116.1:c.15398C>G	XP_011539418.1:p.Ser5133Cys
XM_011541117.1:c.15347C>G	XP_011539419.1:p.Ser5116Cys
XM_011541118.1:c.15344C>G	XP_011539420.1:p.Ser5115Cys
XM_011541119.1:c.15311C>G	XP_011539421.1:p.Ser5104Cys
XM_011541120.1:c.15308C>G	XP_011539422.1:p.Ser5103Cys
XM_011541121.1:c.15275C>G	XP_011539423.1:p.Ser5092Cys
XM_011541108.3:c.15545C>G	XP_011539410.2:p.Ser5182Cys
XM_011541109.3:c.15542C>G	XP_011539411.2:p.Ser5181Cys
XM_011541110.3:c.15542C>G	XP_011539412.2:p.Ser5181Cys
XM_011541111.3:c.15542C>G	XP_011539413.2:p.Ser5181Cys
XM_011541112.3:c.15530C>G	XP_011539414.2:p.Ser5177Cys
XM_011541113.3:c.15527C>G	XP_011539415.2:p.Ser5176Cys
XM_011541114.3:c.15527C>G	XP_011539416.2:p.Ser5176Cys
XM_011541115.3:c.15521C>G	XP_011539417.2:p.Ser5174Cys
XM_011541116.3:c.15512C>G	XP_011539418.2:p.Ser5171Cys
XM_011541117.3:c.15461C>G	XP_011539419.2:p.Ser5154Cys
XM_011541118.3:c.15458C>G	XP_011539420.2:p.Ser5153Cys
XM_011541119.3:c.15425C>G	XP_011539421.2:p.Ser5142Cys
XM_011541120.3:c.15422C>G	XP_011539422.2:p.Ser5141Cys
XM_011541121.3:c.15389C>G	XP_011539423.2:p.Ser5130Cys
XM_017000822.2:c.15524C>G	XP_016856311.2:p.Ser5175Cys
XM_017000823.2:c.15497C>G	XP_016856312.2:p.Ser5166Cys
XM_017000824.2:c.15443C>G	XP_016856313.2:p.Ser5148Cys
XM_017000825.2:c.15428C>G	XP_016856314.2:p.Ser5143Cys
XM_017000826.2:c.15425C>G	XP_016856315.2:p.Ser5142Cys
XM_017000827.2:c.15410C>G	XP_016856316.2:p.Ser5137Cys
XM_017000828.2:c.15386C>G	XP_016856317.2:p.Ser5129Cys
XM_017000829.2:c.15338C>G	XP_016856318.2:p.Ser5113Cys
XM_017000830.2:c.15287C>G	XP_016856319.2:p.Ser5096Cys
NM_020765.3:c.15278C>G MANE Select	NP_065816.2:p.Ser5093Cys