Canonical Allele Identifier: CA338748172

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15283C>G MANE Select	ENSP00000364403.3:p.Leu5095Val
ENST00000375224.1:c.2404C>G	ENSP00000364372.1:p.Leu802Val
ENST00000375225.7:c.508C>G	ENSP00000364373.3:p.Leu170Val
ENST00000375254.7:c.15283C>G	ENSP00000364403.3:p.Leu5095Val
ENST00000459947.5:n.3290C>G
NM_020765.2:c.15283C>G	NP_065816.2:p.Leu5095Val
XM_011541108.1:c.15436C>G	XP_011539410.1:p.Leu5146Val
XM_011541109.1:c.15433C>G	XP_011539411.1:p.Leu5145Val
XM_011541110.1:c.15433C>G	XP_011539412.1:p.Leu5145Val
XM_011541111.1:c.15433C>G	XP_011539413.1:p.Leu5145Val
XM_011541112.1:c.15421C>G	XP_011539414.1:p.Leu5141Val
XM_011541113.1:c.15418C>G	XP_011539415.1:p.Leu5140Val
XM_011541114.1:c.15418C>G	XP_011539416.1:p.Leu5140Val
XM_011541115.1:c.15412C>G	XP_011539417.1:p.Leu5138Val
XM_011541116.1:c.15403C>G	XP_011539418.1:p.Leu5135Val
XM_011541117.1:c.15352C>G	XP_011539419.1:p.Leu5118Val
XM_011541118.1:c.15349C>G	XP_011539420.1:p.Leu5117Val
XM_011541119.1:c.15316C>G	XP_011539421.1:p.Leu5106Val
XM_011541120.1:c.15313C>G	XP_011539422.1:p.Leu5105Val
XM_011541121.1:c.15280C>G	XP_011539423.1:p.Leu5094Val
XM_011541108.3:c.15550C>G	XP_011539410.2:p.Leu5184Val
XM_011541109.3:c.15547C>G	XP_011539411.2:p.Leu5183Val
XM_011541110.3:c.15547C>G	XP_011539412.2:p.Leu5183Val
XM_011541111.3:c.15547C>G	XP_011539413.2:p.Leu5183Val
XM_011541112.3:c.15535C>G	XP_011539414.2:p.Leu5179Val
XM_011541113.3:c.15532C>G	XP_011539415.2:p.Leu5178Val
XM_011541114.3:c.15532C>G	XP_011539416.2:p.Leu5178Val
XM_011541115.3:c.15526C>G	XP_011539417.2:p.Leu5176Val
XM_011541116.3:c.15517C>G	XP_011539418.2:p.Leu5173Val
XM_011541117.3:c.15466C>G	XP_011539419.2:p.Leu5156Val
XM_011541118.3:c.15463C>G	XP_011539420.2:p.Leu5155Val
XM_011541119.3:c.15430C>G	XP_011539421.2:p.Leu5144Val
XM_011541120.3:c.15427C>G	XP_011539422.2:p.Leu5143Val
XM_011541121.3:c.15394C>G	XP_011539423.2:p.Leu5132Val
XM_017000822.2:c.15529C>G	XP_016856311.2:p.Leu5177Val
XM_017000823.2:c.15502C>G	XP_016856312.2:p.Leu5168Val
XM_017000824.2:c.15448C>G	XP_016856313.2:p.Leu5150Val
XM_017000825.2:c.15433C>G	XP_016856314.2:p.Leu5145Val
XM_017000826.2:c.15430C>G	XP_016856315.2:p.Leu5144Val
XM_017000827.2:c.15415C>G	XP_016856316.2:p.Leu5139Val
XM_017000828.2:c.15391C>G	XP_016856317.2:p.Leu5131Val
XM_017000829.2:c.15343C>G	XP_016856318.2:p.Leu5115Val
XM_017000830.2:c.15292C>G	XP_016856319.2:p.Leu5098Val
NM_020765.3:c.15283C>G MANE Select	NP_065816.2:p.Leu5095Val