Canonical Allele Identifier: CA338748255

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404532A>G (hg19) ; chr1:g.19078038A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078038A>G , CM000663.2:g.19078038A>G	GRCh38
NC_000001.10:g.19404532A>G , CM000663.1:g.19404532A>G	GRCh37
NC_000001.9:g.19277119A>G	NCBI36
NG_027669.1:g.137215T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15262T>C MANE Select	ENSP00000364403.3:p.Ser5088Pro
ENST00000375224.1:c.2383T>C	ENSP00000364372.1:p.Ser795Pro
ENST00000375225.7:c.487T>C	ENSP00000364373.3:p.Ser163Pro
ENST00000375254.7:c.15262T>C	ENSP00000364403.3:p.Ser5088Pro
ENST00000459947.5:n.3269T>C
NM_020765.2:c.15262T>C	NP_065816.2:p.Ser5088Pro
XM_011541108.1:c.15415T>C	XP_011539410.1:p.Ser5139Pro
XM_011541109.1:c.15412T>C	XP_011539411.1:p.Ser5138Pro
XM_011541110.1:c.15412T>C	XP_011539412.1:p.Ser5138Pro
XM_011541111.1:c.15412T>C	XP_011539413.1:p.Ser5138Pro
XM_011541112.1:c.15400T>C	XP_011539414.1:p.Ser5134Pro
XM_011541113.1:c.15397T>C	XP_011539415.1:p.Ser5133Pro
XM_011541114.1:c.15397T>C	XP_011539416.1:p.Ser5133Pro
XM_011541115.1:c.15391T>C	XP_011539417.1:p.Ser5131Pro
XM_011541116.1:c.15382T>C	XP_011539418.1:p.Ser5128Pro
XM_011541117.1:c.15331T>C	XP_011539419.1:p.Ser5111Pro
XM_011541118.1:c.15328T>C	XP_011539420.1:p.Ser5110Pro
XM_011541119.1:c.15295T>C	XP_011539421.1:p.Ser5099Pro
XM_011541120.1:c.15292T>C	XP_011539422.1:p.Ser5098Pro
XM_011541121.1:c.15259T>C	XP_011539423.1:p.Ser5087Pro
XM_011541108.3:c.15529T>C	XP_011539410.2:p.Ser5177Pro
XM_011541109.3:c.15526T>C	XP_011539411.2:p.Ser5176Pro
XM_011541110.3:c.15526T>C	XP_011539412.2:p.Ser5176Pro
XM_011541111.3:c.15526T>C	XP_011539413.2:p.Ser5176Pro
XM_011541112.3:c.15514T>C	XP_011539414.2:p.Ser5172Pro
XM_011541113.3:c.15511T>C	XP_011539415.2:p.Ser5171Pro
XM_011541114.3:c.15511T>C	XP_011539416.2:p.Ser5171Pro
XM_011541115.3:c.15505T>C	XP_011539417.2:p.Ser5169Pro
XM_011541116.3:c.15496T>C	XP_011539418.2:p.Ser5166Pro
XM_011541117.3:c.15445T>C	XP_011539419.2:p.Ser5149Pro
XM_011541118.3:c.15442T>C	XP_011539420.2:p.Ser5148Pro
XM_011541119.3:c.15409T>C	XP_011539421.2:p.Ser5137Pro
XM_011541120.3:c.15406T>C	XP_011539422.2:p.Ser5136Pro
XM_011541121.3:c.15373T>C	XP_011539423.2:p.Ser5125Pro
XM_017000822.2:c.15508T>C	XP_016856311.2:p.Ser5170Pro
XM_017000823.2:c.15481T>C	XP_016856312.2:p.Ser5161Pro
XM_017000824.2:c.15427T>C	XP_016856313.2:p.Ser5143Pro
XM_017000825.2:c.15412T>C	XP_016856314.2:p.Ser5138Pro
XM_017000826.2:c.15409T>C	XP_016856315.2:p.Ser5137Pro
XM_017000827.2:c.15394T>C	XP_016856316.2:p.Ser5132Pro
XM_017000828.2:c.15370T>C	XP_016856317.2:p.Ser5124Pro
XM_017000829.2:c.15322T>C	XP_016856318.2:p.Ser5108Pro
XM_017000830.2:c.15271T>C	XP_016856319.2:p.Ser5091Pro
NM_020765.3:c.15262T>C MANE Select	NP_065816.2:p.Ser5088Pro