Canonical Allele Identifier: CA338748282

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404538C>A (hg19) ; chr1:g.19078044C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078044C>A , CM000663.2:g.19078044C>A	GRCh38
NC_000001.10:g.19404538C>A , CM000663.1:g.19404538C>A	GRCh37
NC_000001.9:g.19277125C>A	NCBI36
NG_027669.1:g.137209G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15256G>T MANE Select	ENSP00000364403.3:p.Asp5086Tyr
ENST00000375224.1:c.2377G>T	ENSP00000364372.1:p.Asp793Tyr
ENST00000375225.7:c.481G>T	ENSP00000364373.3:p.Asp161Tyr
ENST00000375254.7:c.15256G>T	ENSP00000364403.3:p.Asp5086Tyr
ENST00000459947.5:n.3263G>T
NM_020765.2:c.15256G>T	NP_065816.2:p.Asp5086Tyr
XM_011541108.1:c.15409G>T	XP_011539410.1:p.Asp5137Tyr
XM_011541109.1:c.15406G>T	XP_011539411.1:p.Asp5136Tyr
XM_011541110.1:c.15406G>T	XP_011539412.1:p.Asp5136Tyr
XM_011541111.1:c.15406G>T	XP_011539413.1:p.Asp5136Tyr
XM_011541112.1:c.15394G>T	XP_011539414.1:p.Asp5132Tyr
XM_011541113.1:c.15391G>T	XP_011539415.1:p.Asp5131Tyr
XM_011541114.1:c.15391G>T	XP_011539416.1:p.Asp5131Tyr
XM_011541115.1:c.15385G>T	XP_011539417.1:p.Asp5129Tyr
XM_011541116.1:c.15376G>T	XP_011539418.1:p.Asp5126Tyr
XM_011541117.1:c.15325G>T	XP_011539419.1:p.Asp5109Tyr
XM_011541118.1:c.15322G>T	XP_011539420.1:p.Asp5108Tyr
XM_011541119.1:c.15289G>T	XP_011539421.1:p.Asp5097Tyr
XM_011541120.1:c.15286G>T	XP_011539422.1:p.Asp5096Tyr
XM_011541121.1:c.15253G>T	XP_011539423.1:p.Asp5085Tyr
XM_011541108.3:c.15523G>T	XP_011539410.2:p.Asp5175Tyr
XM_011541109.3:c.15520G>T	XP_011539411.2:p.Asp5174Tyr
XM_011541110.3:c.15520G>T	XP_011539412.2:p.Asp5174Tyr
XM_011541111.3:c.15520G>T	XP_011539413.2:p.Asp5174Tyr
XM_011541112.3:c.15508G>T	XP_011539414.2:p.Asp5170Tyr
XM_011541113.3:c.15505G>T	XP_011539415.2:p.Asp5169Tyr
XM_011541114.3:c.15505G>T	XP_011539416.2:p.Asp5169Tyr
XM_011541115.3:c.15499G>T	XP_011539417.2:p.Asp5167Tyr
XM_011541116.3:c.15490G>T	XP_011539418.2:p.Asp5164Tyr
XM_011541117.3:c.15439G>T	XP_011539419.2:p.Asp5147Tyr
XM_011541118.3:c.15436G>T	XP_011539420.2:p.Asp5146Tyr
XM_011541119.3:c.15403G>T	XP_011539421.2:p.Asp5135Tyr
XM_011541120.3:c.15400G>T	XP_011539422.2:p.Asp5134Tyr
XM_011541121.3:c.15367G>T	XP_011539423.2:p.Asp5123Tyr
XM_017000822.2:c.15502G>T	XP_016856311.2:p.Asp5168Tyr
XM_017000823.2:c.15475G>T	XP_016856312.2:p.Asp5159Tyr
XM_017000824.2:c.15421G>T	XP_016856313.2:p.Asp5141Tyr
XM_017000825.2:c.15406G>T	XP_016856314.2:p.Asp5136Tyr
XM_017000826.2:c.15403G>T	XP_016856315.2:p.Asp5135Tyr
XM_017000827.2:c.15388G>T	XP_016856316.2:p.Asp5130Tyr
XM_017000828.2:c.15364G>T	XP_016856317.2:p.Asp5122Tyr
XM_017000829.2:c.15316G>T	XP_016856318.2:p.Asp5106Tyr
XM_017000830.2:c.15265G>T	XP_016856319.2:p.Asp5089Tyr
NM_020765.3:c.15256G>T MANE Select	NP_065816.2:p.Asp5086Tyr