Canonical Allele Identifier: CA338748310

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404546G>C (hg19) ; chr1:g.19078052G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078052G>C , CM000663.2:g.19078052G>C	GRCh38
NC_000001.10:g.19404546G>C , CM000663.1:g.19404546G>C	GRCh37
NC_000001.9:g.19277133G>C	NCBI36
NG_027669.1:g.137201C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15248C>G MANE Select	ENSP00000364403.3:p.Ala5083Gly
ENST00000375224.1:c.2369C>G	ENSP00000364372.1:p.Ala790Gly
ENST00000375225.7:c.473C>G	ENSP00000364373.3:p.Ala158Gly
ENST00000375254.7:c.15248C>G	ENSP00000364403.3:p.Ala5083Gly
ENST00000459947.5:n.3255C>G
NM_020765.2:c.15248C>G	NP_065816.2:p.Ala5083Gly
XM_011541108.1:c.15401C>G	XP_011539410.1:p.Ala5134Gly
XM_011541109.1:c.15398C>G	XP_011539411.1:p.Ala5133Gly
XM_011541110.1:c.15398C>G	XP_011539412.1:p.Ala5133Gly
XM_011541111.1:c.15398C>G	XP_011539413.1:p.Ala5133Gly
XM_011541112.1:c.15386C>G	XP_011539414.1:p.Ala5129Gly
XM_011541113.1:c.15383C>G	XP_011539415.1:p.Ala5128Gly
XM_011541114.1:c.15383C>G	XP_011539416.1:p.Ala5128Gly
XM_011541115.1:c.15377C>G	XP_011539417.1:p.Ala5126Gly
XM_011541116.1:c.15368C>G	XP_011539418.1:p.Ala5123Gly
XM_011541117.1:c.15317C>G	XP_011539419.1:p.Ala5106Gly
XM_011541118.1:c.15314C>G	XP_011539420.1:p.Ala5105Gly
XM_011541119.1:c.15281C>G	XP_011539421.1:p.Ala5094Gly
XM_011541120.1:c.15278C>G	XP_011539422.1:p.Ala5093Gly
XM_011541121.1:c.15245C>G	XP_011539423.1:p.Ala5082Gly
XM_011541108.3:c.15515C>G	XP_011539410.2:p.Ala5172Gly
XM_011541109.3:c.15512C>G	XP_011539411.2:p.Ala5171Gly
XM_011541110.3:c.15512C>G	XP_011539412.2:p.Ala5171Gly
XM_011541111.3:c.15512C>G	XP_011539413.2:p.Ala5171Gly
XM_011541112.3:c.15500C>G	XP_011539414.2:p.Ala5167Gly
XM_011541113.3:c.15497C>G	XP_011539415.2:p.Ala5166Gly
XM_011541114.3:c.15497C>G	XP_011539416.2:p.Ala5166Gly
XM_011541115.3:c.15491C>G	XP_011539417.2:p.Ala5164Gly
XM_011541116.3:c.15482C>G	XP_011539418.2:p.Ala5161Gly
XM_011541117.3:c.15431C>G	XP_011539419.2:p.Ala5144Gly
XM_011541118.3:c.15428C>G	XP_011539420.2:p.Ala5143Gly
XM_011541119.3:c.15395C>G	XP_011539421.2:p.Ala5132Gly
XM_011541120.3:c.15392C>G	XP_011539422.2:p.Ala5131Gly
XM_011541121.3:c.15359C>G	XP_011539423.2:p.Ala5120Gly
XM_017000822.2:c.15494C>G	XP_016856311.2:p.Ala5165Gly
XM_017000823.2:c.15467C>G	XP_016856312.2:p.Ala5156Gly
XM_017000824.2:c.15413C>G	XP_016856313.2:p.Ala5138Gly
XM_017000825.2:c.15398C>G	XP_016856314.2:p.Ala5133Gly
XM_017000826.2:c.15395C>G	XP_016856315.2:p.Ala5132Gly
XM_017000827.2:c.15380C>G	XP_016856316.2:p.Ala5127Gly
XM_017000828.2:c.15356C>G	XP_016856317.2:p.Ala5119Gly
XM_017000829.2:c.15308C>G	XP_016856318.2:p.Ala5103Gly
XM_017000830.2:c.15257C>G	XP_016856319.2:p.Ala5086Gly
NM_020765.3:c.15248C>G MANE Select	NP_065816.2:p.Ala5083Gly