Canonical Allele Identifier: CA338748280

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404537T>G (hg19) ; chr1:g.19078043T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078043T>G , CM000663.2:g.19078043T>G	GRCh38
NC_000001.10:g.19404537T>G , CM000663.1:g.19404537T>G	GRCh37
NC_000001.9:g.19277124T>G	NCBI36
NG_027669.1:g.137210A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15257A>C MANE Select	ENSP00000364403.3:p.Asp5086Ala
ENST00000375224.1:c.2378A>C	ENSP00000364372.1:p.Asp793Ala
ENST00000375225.7:c.482A>C	ENSP00000364373.3:p.Asp161Ala
ENST00000375254.7:c.15257A>C	ENSP00000364403.3:p.Asp5086Ala
ENST00000459947.5:n.3264A>C
NM_020765.2:c.15257A>C	NP_065816.2:p.Asp5086Ala
XM_011541108.1:c.15410A>C	XP_011539410.1:p.Asp5137Ala
XM_011541109.1:c.15407A>C	XP_011539411.1:p.Asp5136Ala
XM_011541110.1:c.15407A>C	XP_011539412.1:p.Asp5136Ala
XM_011541111.1:c.15407A>C	XP_011539413.1:p.Asp5136Ala
XM_011541112.1:c.15395A>C	XP_011539414.1:p.Asp5132Ala
XM_011541113.1:c.15392A>C	XP_011539415.1:p.Asp5131Ala
XM_011541114.1:c.15392A>C	XP_011539416.1:p.Asp5131Ala
XM_011541115.1:c.15386A>C	XP_011539417.1:p.Asp5129Ala
XM_011541116.1:c.15377A>C	XP_011539418.1:p.Asp5126Ala
XM_011541117.1:c.15326A>C	XP_011539419.1:p.Asp5109Ala
XM_011541118.1:c.15323A>C	XP_011539420.1:p.Asp5108Ala
XM_011541119.1:c.15290A>C	XP_011539421.1:p.Asp5097Ala
XM_011541120.1:c.15287A>C	XP_011539422.1:p.Asp5096Ala
XM_011541121.1:c.15254A>C	XP_011539423.1:p.Asp5085Ala
XM_011541108.3:c.15524A>C	XP_011539410.2:p.Asp5175Ala
XM_011541109.3:c.15521A>C	XP_011539411.2:p.Asp5174Ala
XM_011541110.3:c.15521A>C	XP_011539412.2:p.Asp5174Ala
XM_011541111.3:c.15521A>C	XP_011539413.2:p.Asp5174Ala
XM_011541112.3:c.15509A>C	XP_011539414.2:p.Asp5170Ala
XM_011541113.3:c.15506A>C	XP_011539415.2:p.Asp5169Ala
XM_011541114.3:c.15506A>C	XP_011539416.2:p.Asp5169Ala
XM_011541115.3:c.15500A>C	XP_011539417.2:p.Asp5167Ala
XM_011541116.3:c.15491A>C	XP_011539418.2:p.Asp5164Ala
XM_011541117.3:c.15440A>C	XP_011539419.2:p.Asp5147Ala
XM_011541118.3:c.15437A>C	XP_011539420.2:p.Asp5146Ala
XM_011541119.3:c.15404A>C	XP_011539421.2:p.Asp5135Ala
XM_011541120.3:c.15401A>C	XP_011539422.2:p.Asp5134Ala
XM_011541121.3:c.15368A>C	XP_011539423.2:p.Asp5123Ala
XM_017000822.2:c.15503A>C	XP_016856311.2:p.Asp5168Ala
XM_017000823.2:c.15476A>C	XP_016856312.2:p.Asp5159Ala
XM_017000824.2:c.15422A>C	XP_016856313.2:p.Asp5141Ala
XM_017000825.2:c.15407A>C	XP_016856314.2:p.Asp5136Ala
XM_017000826.2:c.15404A>C	XP_016856315.2:p.Asp5135Ala
XM_017000827.2:c.15389A>C	XP_016856316.2:p.Asp5130Ala
XM_017000828.2:c.15365A>C	XP_016856317.2:p.Asp5122Ala
XM_017000829.2:c.15317A>C	XP_016856318.2:p.Asp5106Ala
XM_017000830.2:c.15266A>C	XP_016856319.2:p.Asp5089Ala
NM_020765.3:c.15257A>C MANE Select	NP_065816.2:p.Asp5086Ala