Canonical Allele Identifier: CA338748125

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404491A>C (hg19) ; chr1:g.19077997A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077997A>C , CM000663.2:g.19077997A>C	GRCh38
NC_000001.10:g.19404491A>C , CM000663.1:g.19404491A>C	GRCh37
NC_000001.9:g.19277078A>C	NCBI36
NG_027669.1:g.137256T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15303T>G MANE Select	ENSP00000364403.3:p.Asp5101Glu
ENST00000375224.1:c.2424T>G	ENSP00000364372.1:p.Asp808Glu
ENST00000375225.7:c.528T>G	ENSP00000364373.3:p.Asp176Glu
ENST00000375254.7:c.15303T>G	ENSP00000364403.3:p.Asp5101Glu
ENST00000459947.5:n.3310T>G
NM_020765.2:c.15303T>G	NP_065816.2:p.Asp5101Glu
XM_011541108.1:c.15456T>G	XP_011539410.1:p.Asp5152Glu
XM_011541109.1:c.15453T>G	XP_011539411.1:p.Asp5151Glu
XM_011541110.1:c.15453T>G	XP_011539412.1:p.Asp5151Glu
XM_011541111.1:c.15453T>G	XP_011539413.1:p.Asp5151Glu
XM_011541112.1:c.15441T>G	XP_011539414.1:p.Asp5147Glu
XM_011541113.1:c.15438T>G	XP_011539415.1:p.Asp5146Glu
XM_011541114.1:c.15438T>G	XP_011539416.1:p.Asp5146Glu
XM_011541115.1:c.15432T>G	XP_011539417.1:p.Asp5144Glu
XM_011541116.1:c.15423T>G	XP_011539418.1:p.Asp5141Glu
XM_011541117.1:c.15372T>G	XP_011539419.1:p.Asp5124Glu
XM_011541118.1:c.15369T>G	XP_011539420.1:p.Asp5123Glu
XM_011541119.1:c.15336T>G	XP_011539421.1:p.Asp5112Glu
XM_011541120.1:c.15333T>G	XP_011539422.1:p.Asp5111Glu
XM_011541121.1:c.15300T>G	XP_011539423.1:p.Asp5100Glu
XM_011541108.3:c.15570T>G	XP_011539410.2:p.Asp5190Glu
XM_011541109.3:c.15567T>G	XP_011539411.2:p.Asp5189Glu
XM_011541110.3:c.15567T>G	XP_011539412.2:p.Asp5189Glu
XM_011541111.3:c.15567T>G	XP_011539413.2:p.Asp5189Glu
XM_011541112.3:c.15555T>G	XP_011539414.2:p.Asp5185Glu
XM_011541113.3:c.15552T>G	XP_011539415.2:p.Asp5184Glu
XM_011541114.3:c.15552T>G	XP_011539416.2:p.Asp5184Glu
XM_011541115.3:c.15546T>G	XP_011539417.2:p.Asp5182Glu
XM_011541116.3:c.15537T>G	XP_011539418.2:p.Asp5179Glu
XM_011541117.3:c.15486T>G	XP_011539419.2:p.Asp5162Glu
XM_011541118.3:c.15483T>G	XP_011539420.2:p.Asp5161Glu
XM_011541119.3:c.15450T>G	XP_011539421.2:p.Asp5150Glu
XM_011541120.3:c.15447T>G	XP_011539422.2:p.Asp5149Glu
XM_011541121.3:c.15414T>G	XP_011539423.2:p.Asp5138Glu
XM_017000822.2:c.15549T>G	XP_016856311.2:p.Asp5183Glu
XM_017000823.2:c.15522T>G	XP_016856312.2:p.Asp5174Glu
XM_017000824.2:c.15468T>G	XP_016856313.2:p.Asp5156Glu
XM_017000825.2:c.15453T>G	XP_016856314.2:p.Asp5151Glu
XM_017000826.2:c.15450T>G	XP_016856315.2:p.Asp5150Glu
XM_017000827.2:c.15435T>G	XP_016856316.2:p.Asp5145Glu
XM_017000828.2:c.15411T>G	XP_016856317.2:p.Asp5137Glu
XM_017000829.2:c.15363T>G	XP_016856318.2:p.Asp5121Glu
XM_017000830.2:c.15312T>G	XP_016856319.2:p.Asp5104Glu
NM_020765.3:c.15303T>G MANE Select	NP_065816.2:p.Asp5101Glu