Canonical Allele Identifier: CA338748272

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404536G>C (hg19) ; chr1:g.19078042G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078042G>C , CM000663.2:g.19078042G>C	GRCh38
NC_000001.10:g.19404536G>C , CM000663.1:g.19404536G>C	GRCh37
NC_000001.9:g.19277123G>C	NCBI36
NG_027669.1:g.137211C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15258C>G MANE Select	ENSP00000364403.3:p.Asp5086Glu
ENST00000375224.1:c.2379C>G	ENSP00000364372.1:p.Asp793Glu
ENST00000375225.7:c.483C>G	ENSP00000364373.3:p.Asp161Glu
ENST00000375254.7:c.15258C>G	ENSP00000364403.3:p.Asp5086Glu
ENST00000459947.5:n.3265C>G
NM_020765.2:c.15258C>G	NP_065816.2:p.Asp5086Glu
XM_011541108.1:c.15411C>G	XP_011539410.1:p.Asp5137Glu
XM_011541109.1:c.15408C>G	XP_011539411.1:p.Asp5136Glu
XM_011541110.1:c.15408C>G	XP_011539412.1:p.Asp5136Glu
XM_011541111.1:c.15408C>G	XP_011539413.1:p.Asp5136Glu
XM_011541112.1:c.15396C>G	XP_011539414.1:p.Asp5132Glu
XM_011541113.1:c.15393C>G	XP_011539415.1:p.Asp5131Glu
XM_011541114.1:c.15393C>G	XP_011539416.1:p.Asp5131Glu
XM_011541115.1:c.15387C>G	XP_011539417.1:p.Asp5129Glu
XM_011541116.1:c.15378C>G	XP_011539418.1:p.Asp5126Glu
XM_011541117.1:c.15327C>G	XP_011539419.1:p.Asp5109Glu
XM_011541118.1:c.15324C>G	XP_011539420.1:p.Asp5108Glu
XM_011541119.1:c.15291C>G	XP_011539421.1:p.Asp5097Glu
XM_011541120.1:c.15288C>G	XP_011539422.1:p.Asp5096Glu
XM_011541121.1:c.15255C>G	XP_011539423.1:p.Asp5085Glu
XM_011541108.3:c.15525C>G	XP_011539410.2:p.Asp5175Glu
XM_011541109.3:c.15522C>G	XP_011539411.2:p.Asp5174Glu
XM_011541110.3:c.15522C>G	XP_011539412.2:p.Asp5174Glu
XM_011541111.3:c.15522C>G	XP_011539413.2:p.Asp5174Glu
XM_011541112.3:c.15510C>G	XP_011539414.2:p.Asp5170Glu
XM_011541113.3:c.15507C>G	XP_011539415.2:p.Asp5169Glu
XM_011541114.3:c.15507C>G	XP_011539416.2:p.Asp5169Glu
XM_011541115.3:c.15501C>G	XP_011539417.2:p.Asp5167Glu
XM_011541116.3:c.15492C>G	XP_011539418.2:p.Asp5164Glu
XM_011541117.3:c.15441C>G	XP_011539419.2:p.Asp5147Glu
XM_011541118.3:c.15438C>G	XP_011539420.2:p.Asp5146Glu
XM_011541119.3:c.15405C>G	XP_011539421.2:p.Asp5135Glu
XM_011541120.3:c.15402C>G	XP_011539422.2:p.Asp5134Glu
XM_011541121.3:c.15369C>G	XP_011539423.2:p.Asp5123Glu
XM_017000822.2:c.15504C>G	XP_016856311.2:p.Asp5168Glu
XM_017000823.2:c.15477C>G	XP_016856312.2:p.Asp5159Glu
XM_017000824.2:c.15423C>G	XP_016856313.2:p.Asp5141Glu
XM_017000825.2:c.15408C>G	XP_016856314.2:p.Asp5136Glu
XM_017000826.2:c.15405C>G	XP_016856315.2:p.Asp5135Glu
XM_017000827.2:c.15390C>G	XP_016856316.2:p.Asp5130Glu
XM_017000828.2:c.15366C>G	XP_016856317.2:p.Asp5122Glu
XM_017000829.2:c.15318C>G	XP_016856318.2:p.Asp5106Glu
XM_017000830.2:c.15267C>G	XP_016856319.2:p.Asp5089Glu
NM_020765.3:c.15258C>G MANE Select	NP_065816.2:p.Asp5086Glu