Canonical Allele Identifier: CA338748170

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404511G>A (hg19) ; chr1:g.19078017G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078017G>A , CM000663.2:g.19078017G>A	GRCh38
NC_000001.10:g.19404511G>A , CM000663.1:g.19404511G>A	GRCh37
NC_000001.9:g.19277098G>A	NCBI36
NG_027669.1:g.137236C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15283C>T MANE Select	ENSP00000364403.3:p.Leu5095Phe
ENST00000375224.1:c.2404C>T	ENSP00000364372.1:p.Leu802Phe
ENST00000375225.7:c.508C>T	ENSP00000364373.3:p.Leu170Phe
ENST00000375254.7:c.15283C>T	ENSP00000364403.3:p.Leu5095Phe
ENST00000459947.5:n.3290C>T
NM_020765.2:c.15283C>T	NP_065816.2:p.Leu5095Phe
XM_011541108.1:c.15436C>T	XP_011539410.1:p.Leu5146Phe
XM_011541109.1:c.15433C>T	XP_011539411.1:p.Leu5145Phe
XM_011541110.1:c.15433C>T	XP_011539412.1:p.Leu5145Phe
XM_011541111.1:c.15433C>T	XP_011539413.1:p.Leu5145Phe
XM_011541112.1:c.15421C>T	XP_011539414.1:p.Leu5141Phe
XM_011541113.1:c.15418C>T	XP_011539415.1:p.Leu5140Phe
XM_011541114.1:c.15418C>T	XP_011539416.1:p.Leu5140Phe
XM_011541115.1:c.15412C>T	XP_011539417.1:p.Leu5138Phe
XM_011541116.1:c.15403C>T	XP_011539418.1:p.Leu5135Phe
XM_011541117.1:c.15352C>T	XP_011539419.1:p.Leu5118Phe
XM_011541118.1:c.15349C>T	XP_011539420.1:p.Leu5117Phe
XM_011541119.1:c.15316C>T	XP_011539421.1:p.Leu5106Phe
XM_011541120.1:c.15313C>T	XP_011539422.1:p.Leu5105Phe
XM_011541121.1:c.15280C>T	XP_011539423.1:p.Leu5094Phe
XM_011541108.3:c.15550C>T	XP_011539410.2:p.Leu5184Phe
XM_011541109.3:c.15547C>T	XP_011539411.2:p.Leu5183Phe
XM_011541110.3:c.15547C>T	XP_011539412.2:p.Leu5183Phe
XM_011541111.3:c.15547C>T	XP_011539413.2:p.Leu5183Phe
XM_011541112.3:c.15535C>T	XP_011539414.2:p.Leu5179Phe
XM_011541113.3:c.15532C>T	XP_011539415.2:p.Leu5178Phe
XM_011541114.3:c.15532C>T	XP_011539416.2:p.Leu5178Phe
XM_011541115.3:c.15526C>T	XP_011539417.2:p.Leu5176Phe
XM_011541116.3:c.15517C>T	XP_011539418.2:p.Leu5173Phe
XM_011541117.3:c.15466C>T	XP_011539419.2:p.Leu5156Phe
XM_011541118.3:c.15463C>T	XP_011539420.2:p.Leu5155Phe
XM_011541119.3:c.15430C>T	XP_011539421.2:p.Leu5144Phe
XM_011541120.3:c.15427C>T	XP_011539422.2:p.Leu5143Phe
XM_011541121.3:c.15394C>T	XP_011539423.2:p.Leu5132Phe
XM_017000822.2:c.15529C>T	XP_016856311.2:p.Leu5177Phe
XM_017000823.2:c.15502C>T	XP_016856312.2:p.Leu5168Phe
XM_017000824.2:c.15448C>T	XP_016856313.2:p.Leu5150Phe
XM_017000825.2:c.15433C>T	XP_016856314.2:p.Leu5145Phe
XM_017000826.2:c.15430C>T	XP_016856315.2:p.Leu5144Phe
XM_017000827.2:c.15415C>T	XP_016856316.2:p.Leu5139Phe
XM_017000828.2:c.15391C>T	XP_016856317.2:p.Leu5131Phe
XM_017000829.2:c.15343C>T	XP_016856318.2:p.Leu5115Phe
XM_017000830.2:c.15292C>T	XP_016856319.2:p.Leu5098Phe
NM_020765.3:c.15283C>T MANE Select	NP_065816.2:p.Leu5095Phe