Canonical Allele Identifier: CA338748267

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404535A>C (hg19) ; chr1:g.19078041A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078041A>C , CM000663.2:g.19078041A>C	GRCh38
NC_000001.10:g.19404535A>C , CM000663.1:g.19404535A>C	GRCh37
NC_000001.9:g.19277122A>C	NCBI36
NG_027669.1:g.137212T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15259T>G MANE Select	ENSP00000364403.3:p.Tyr5087Asp
ENST00000375224.1:c.2380T>G	ENSP00000364372.1:p.Tyr794Asp
ENST00000375225.7:c.484T>G	ENSP00000364373.3:p.Tyr162Asp
ENST00000375254.7:c.15259T>G	ENSP00000364403.3:p.Tyr5087Asp
ENST00000459947.5:n.3266T>G
NM_020765.2:c.15259T>G	NP_065816.2:p.Tyr5087Asp
XM_011541108.1:c.15412T>G	XP_011539410.1:p.Tyr5138Asp
XM_011541109.1:c.15409T>G	XP_011539411.1:p.Tyr5137Asp
XM_011541110.1:c.15409T>G	XP_011539412.1:p.Tyr5137Asp
XM_011541111.1:c.15409T>G	XP_011539413.1:p.Tyr5137Asp
XM_011541112.1:c.15397T>G	XP_011539414.1:p.Tyr5133Asp
XM_011541113.1:c.15394T>G	XP_011539415.1:p.Tyr5132Asp
XM_011541114.1:c.15394T>G	XP_011539416.1:p.Tyr5132Asp
XM_011541115.1:c.15388T>G	XP_011539417.1:p.Tyr5130Asp
XM_011541116.1:c.15379T>G	XP_011539418.1:p.Tyr5127Asp
XM_011541117.1:c.15328T>G	XP_011539419.1:p.Tyr5110Asp
XM_011541118.1:c.15325T>G	XP_011539420.1:p.Tyr5109Asp
XM_011541119.1:c.15292T>G	XP_011539421.1:p.Tyr5098Asp
XM_011541120.1:c.15289T>G	XP_011539422.1:p.Tyr5097Asp
XM_011541121.1:c.15256T>G	XP_011539423.1:p.Tyr5086Asp
XM_011541108.3:c.15526T>G	XP_011539410.2:p.Tyr5176Asp
XM_011541109.3:c.15523T>G	XP_011539411.2:p.Tyr5175Asp
XM_011541110.3:c.15523T>G	XP_011539412.2:p.Tyr5175Asp
XM_011541111.3:c.15523T>G	XP_011539413.2:p.Tyr5175Asp
XM_011541112.3:c.15511T>G	XP_011539414.2:p.Tyr5171Asp
XM_011541113.3:c.15508T>G	XP_011539415.2:p.Tyr5170Asp
XM_011541114.3:c.15508T>G	XP_011539416.2:p.Tyr5170Asp
XM_011541115.3:c.15502T>G	XP_011539417.2:p.Tyr5168Asp
XM_011541116.3:c.15493T>G	XP_011539418.2:p.Tyr5165Asp
XM_011541117.3:c.15442T>G	XP_011539419.2:p.Tyr5148Asp
XM_011541118.3:c.15439T>G	XP_011539420.2:p.Tyr5147Asp
XM_011541119.3:c.15406T>G	XP_011539421.2:p.Tyr5136Asp
XM_011541120.3:c.15403T>G	XP_011539422.2:p.Tyr5135Asp
XM_011541121.3:c.15370T>G	XP_011539423.2:p.Tyr5124Asp
XM_017000822.2:c.15505T>G	XP_016856311.2:p.Tyr5169Asp
XM_017000823.2:c.15478T>G	XP_016856312.2:p.Tyr5160Asp
XM_017000824.2:c.15424T>G	XP_016856313.2:p.Tyr5142Asp
XM_017000825.2:c.15409T>G	XP_016856314.2:p.Tyr5137Asp
XM_017000826.2:c.15406T>G	XP_016856315.2:p.Tyr5136Asp
XM_017000827.2:c.15391T>G	XP_016856316.2:p.Tyr5131Asp
XM_017000828.2:c.15367T>G	XP_016856317.2:p.Tyr5123Asp
XM_017000829.2:c.15319T>G	XP_016856318.2:p.Tyr5107Asp
XM_017000830.2:c.15268T>G	XP_016856319.2:p.Tyr5090Asp
NM_020765.3:c.15259T>G MANE Select	NP_065816.2:p.Tyr5087Asp