Canonical Allele Identifier: CA338748336

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404552T>A (hg19) ; chr1:g.19078058T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078058T>A , CM000663.2:g.19078058T>A	GRCh38
NC_000001.10:g.19404552T>A , CM000663.1:g.19404552T>A	GRCh37
NC_000001.9:g.19277139T>A	NCBI36
NG_027669.1:g.137195A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15242A>T MANE Select	ENSP00000364403.3:p.Asp5081Val
ENST00000375224.1:c.2363A>T	ENSP00000364372.1:p.Asp788Val
ENST00000375225.7:c.467A>T	ENSP00000364373.3:p.Asp156Val
ENST00000375254.7:c.15242A>T	ENSP00000364403.3:p.Asp5081Val
ENST00000459947.5:n.3249A>T
NM_020765.2:c.15242A>T	NP_065816.2:p.Asp5081Val
XM_011541108.1:c.15395A>T	XP_011539410.1:p.Asp5132Val
XM_011541109.1:c.15392A>T	XP_011539411.1:p.Asp5131Val
XM_011541110.1:c.15392A>T	XP_011539412.1:p.Asp5131Val
XM_011541111.1:c.15392A>T	XP_011539413.1:p.Asp5131Val
XM_011541112.1:c.15380A>T	XP_011539414.1:p.Asp5127Val
XM_011541113.1:c.15377A>T	XP_011539415.1:p.Asp5126Val
XM_011541114.1:c.15377A>T	XP_011539416.1:p.Asp5126Val
XM_011541115.1:c.15371A>T	XP_011539417.1:p.Asp5124Val
XM_011541116.1:c.15362A>T	XP_011539418.1:p.Asp5121Val
XM_011541117.1:c.15311A>T	XP_011539419.1:p.Asp5104Val
XM_011541118.1:c.15308A>T	XP_011539420.1:p.Asp5103Val
XM_011541119.1:c.15275A>T	XP_011539421.1:p.Asp5092Val
XM_011541120.1:c.15272A>T	XP_011539422.1:p.Asp5091Val
XM_011541121.1:c.15239A>T	XP_011539423.1:p.Asp5080Val
XM_011541108.3:c.15509A>T	XP_011539410.2:p.Asp5170Val
XM_011541109.3:c.15506A>T	XP_011539411.2:p.Asp5169Val
XM_011541110.3:c.15506A>T	XP_011539412.2:p.Asp5169Val
XM_011541111.3:c.15506A>T	XP_011539413.2:p.Asp5169Val
XM_011541112.3:c.15494A>T	XP_011539414.2:p.Asp5165Val
XM_011541113.3:c.15491A>T	XP_011539415.2:p.Asp5164Val
XM_011541114.3:c.15491A>T	XP_011539416.2:p.Asp5164Val
XM_011541115.3:c.15485A>T	XP_011539417.2:p.Asp5162Val
XM_011541116.3:c.15476A>T	XP_011539418.2:p.Asp5159Val
XM_011541117.3:c.15425A>T	XP_011539419.2:p.Asp5142Val
XM_011541118.3:c.15422A>T	XP_011539420.2:p.Asp5141Val
XM_011541119.3:c.15389A>T	XP_011539421.2:p.Asp5130Val
XM_011541120.3:c.15386A>T	XP_011539422.2:p.Asp5129Val
XM_011541121.3:c.15353A>T	XP_011539423.2:p.Asp5118Val
XM_017000822.2:c.15488A>T	XP_016856311.2:p.Asp5163Val
XM_017000823.2:c.15461A>T	XP_016856312.2:p.Asp5154Val
XM_017000824.2:c.15407A>T	XP_016856313.2:p.Asp5136Val
XM_017000825.2:c.15392A>T	XP_016856314.2:p.Asp5131Val
XM_017000826.2:c.15389A>T	XP_016856315.2:p.Asp5130Val
XM_017000827.2:c.15374A>T	XP_016856316.2:p.Asp5125Val
XM_017000828.2:c.15350A>T	XP_016856317.2:p.Asp5117Val
XM_017000829.2:c.15302A>T	XP_016856318.2:p.Asp5101Val
XM_017000830.2:c.15251A>T	XP_016856319.2:p.Asp5084Val
NM_020765.3:c.15242A>T MANE Select	NP_065816.2:p.Asp5081Val