Canonical Allele Identifier: CA338748317

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404547C>A (hg19) ; chr1:g.19078053C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078053C>A , CM000663.2:g.19078053C>A	GRCh38
NC_000001.10:g.19404547C>A , CM000663.1:g.19404547C>A	GRCh37
NC_000001.9:g.19277134C>A	NCBI36
NG_027669.1:g.137200G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15247G>T MANE Select	ENSP00000364403.3:p.Ala5083Ser
ENST00000375224.1:c.2368G>T	ENSP00000364372.1:p.Ala790Ser
ENST00000375225.7:c.472G>T	ENSP00000364373.3:p.Ala158Ser
ENST00000375254.7:c.15247G>T	ENSP00000364403.3:p.Ala5083Ser
ENST00000459947.5:n.3254G>T
NM_020765.2:c.15247G>T	NP_065816.2:p.Ala5083Ser
XM_011541108.1:c.15400G>T	XP_011539410.1:p.Ala5134Ser
XM_011541109.1:c.15397G>T	XP_011539411.1:p.Ala5133Ser
XM_011541110.1:c.15397G>T	XP_011539412.1:p.Ala5133Ser
XM_011541111.1:c.15397G>T	XP_011539413.1:p.Ala5133Ser
XM_011541112.1:c.15385G>T	XP_011539414.1:p.Ala5129Ser
XM_011541113.1:c.15382G>T	XP_011539415.1:p.Ala5128Ser
XM_011541114.1:c.15382G>T	XP_011539416.1:p.Ala5128Ser
XM_011541115.1:c.15376G>T	XP_011539417.1:p.Ala5126Ser
XM_011541116.1:c.15367G>T	XP_011539418.1:p.Ala5123Ser
XM_011541117.1:c.15316G>T	XP_011539419.1:p.Ala5106Ser
XM_011541118.1:c.15313G>T	XP_011539420.1:p.Ala5105Ser
XM_011541119.1:c.15280G>T	XP_011539421.1:p.Ala5094Ser
XM_011541120.1:c.15277G>T	XP_011539422.1:p.Ala5093Ser
XM_011541121.1:c.15244G>T	XP_011539423.1:p.Ala5082Ser
XM_011541108.3:c.15514G>T	XP_011539410.2:p.Ala5172Ser
XM_011541109.3:c.15511G>T	XP_011539411.2:p.Ala5171Ser
XM_011541110.3:c.15511G>T	XP_011539412.2:p.Ala5171Ser
XM_011541111.3:c.15511G>T	XP_011539413.2:p.Ala5171Ser
XM_011541112.3:c.15499G>T	XP_011539414.2:p.Ala5167Ser
XM_011541113.3:c.15496G>T	XP_011539415.2:p.Ala5166Ser
XM_011541114.3:c.15496G>T	XP_011539416.2:p.Ala5166Ser
XM_011541115.3:c.15490G>T	XP_011539417.2:p.Ala5164Ser
XM_011541116.3:c.15481G>T	XP_011539418.2:p.Ala5161Ser
XM_011541117.3:c.15430G>T	XP_011539419.2:p.Ala5144Ser
XM_011541118.3:c.15427G>T	XP_011539420.2:p.Ala5143Ser
XM_011541119.3:c.15394G>T	XP_011539421.2:p.Ala5132Ser
XM_011541120.3:c.15391G>T	XP_011539422.2:p.Ala5131Ser
XM_011541121.3:c.15358G>T	XP_011539423.2:p.Ala5120Ser
XM_017000822.2:c.15493G>T	XP_016856311.2:p.Ala5165Ser
XM_017000823.2:c.15466G>T	XP_016856312.2:p.Ala5156Ser
XM_017000824.2:c.15412G>T	XP_016856313.2:p.Ala5138Ser
XM_017000825.2:c.15397G>T	XP_016856314.2:p.Ala5133Ser
XM_017000826.2:c.15394G>T	XP_016856315.2:p.Ala5132Ser
XM_017000827.2:c.15379G>T	XP_016856316.2:p.Ala5127Ser
XM_017000828.2:c.15355G>T	XP_016856317.2:p.Ala5119Ser
XM_017000829.2:c.15307G>T	XP_016856318.2:p.Ala5103Ser
XM_017000830.2:c.15256G>T	XP_016856319.2:p.Ala5086Ser
NM_020765.3:c.15247G>T MANE Select	NP_065816.2:p.Ala5083Ser