Canonical Allele Identifier: CA18791090

Gene: UBR4

Linked Data

• dbSNP Id: rs552106516
• MyVariant Identifiers: chr1:g.19404558A>T (hg19) ; chr1:g.19078064A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078064A>T , CM000663.2:g.19078064A>T	GRCh38
NC_000001.10:g.19404558A>T , CM000663.1:g.19404558A>T	GRCh37
NC_000001.9:g.19277145A>T	NCBI36
NG_027669.1:g.137189T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15236T>A MANE Select	ENSP00000364403.3:p.Leu5079Gln
ENST00000375224.1:c.2357T>A	ENSP00000364372.1:p.Leu786Gln
ENST00000375225.7:c.461T>A	ENSP00000364373.3:p.Leu154Gln
ENST00000375254.7:c.15236T>A	ENSP00000364403.3:p.Leu5079Gln
ENST00000459947.5:n.3243T>A
NM_020765.2:c.15236T>A	NP_065816.2:p.Leu5079Gln
XM_011541108.1:c.15389T>A	XP_011539410.1:p.Leu5130Gln
XM_011541109.1:c.15386T>A	XP_011539411.1:p.Leu5129Gln
XM_011541110.1:c.15386T>A	XP_011539412.1:p.Leu5129Gln
XM_011541111.1:c.15386T>A	XP_011539413.1:p.Leu5129Gln
XM_011541112.1:c.15374T>A	XP_011539414.1:p.Leu5125Gln
XM_011541113.1:c.15371T>A	XP_011539415.1:p.Leu5124Gln
XM_011541114.1:c.15371T>A	XP_011539416.1:p.Leu5124Gln
XM_011541115.1:c.15365T>A	XP_011539417.1:p.Leu5122Gln
XM_011541116.1:c.15356T>A	XP_011539418.1:p.Leu5119Gln
XM_011541117.1:c.15305T>A	XP_011539419.1:p.Leu5102Gln
XM_011541118.1:c.15302T>A	XP_011539420.1:p.Leu5101Gln
XM_011541119.1:c.15269T>A	XP_011539421.1:p.Leu5090Gln
XM_011541120.1:c.15266T>A	XP_011539422.1:p.Leu5089Gln
XM_011541121.1:c.15233T>A	XP_011539423.1:p.Leu5078Gln
XM_011541108.3:c.15503T>A	XP_011539410.2:p.Leu5168Gln
XM_011541109.3:c.15500T>A	XP_011539411.2:p.Leu5167Gln
XM_011541110.3:c.15500T>A	XP_011539412.2:p.Leu5167Gln
XM_011541111.3:c.15500T>A	XP_011539413.2:p.Leu5167Gln
XM_011541112.3:c.15488T>A	XP_011539414.2:p.Leu5163Gln
XM_011541113.3:c.15485T>A	XP_011539415.2:p.Leu5162Gln
XM_011541114.3:c.15485T>A	XP_011539416.2:p.Leu5162Gln
XM_011541115.3:c.15479T>A	XP_011539417.2:p.Leu5160Gln
XM_011541116.3:c.15470T>A	XP_011539418.2:p.Leu5157Gln
XM_011541117.3:c.15419T>A	XP_011539419.2:p.Leu5140Gln
XM_011541118.3:c.15416T>A	XP_011539420.2:p.Leu5139Gln
XM_011541119.3:c.15383T>A	XP_011539421.2:p.Leu5128Gln
XM_011541120.3:c.15380T>A	XP_011539422.2:p.Leu5127Gln
XM_011541121.3:c.15347T>A	XP_011539423.2:p.Leu5116Gln
XM_017000822.2:c.15482T>A	XP_016856311.2:p.Leu5161Gln
XM_017000823.2:c.15455T>A	XP_016856312.2:p.Leu5152Gln
XM_017000824.2:c.15401T>A	XP_016856313.2:p.Leu5134Gln
XM_017000825.2:c.15386T>A	XP_016856314.2:p.Leu5129Gln
XM_017000826.2:c.15383T>A	XP_016856315.2:p.Leu5128Gln
XM_017000827.2:c.15368T>A	XP_016856316.2:p.Leu5123Gln
XM_017000828.2:c.15344T>A	XP_016856317.2:p.Leu5115Gln
XM_017000829.2:c.15296T>A	XP_016856318.2:p.Leu5099Gln
XM_017000830.2:c.15245T>A	XP_016856319.2:p.Leu5082Gln
NM_020765.3:c.15236T>A MANE Select	NP_065816.2:p.Leu5079Gln