Canonical Allele Identifier: CA338748143

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404499G>C (hg19) ; chr1:g.19078005G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078005G>C , CM000663.2:g.19078005G>C	GRCh38
NC_000001.10:g.19404499G>C , CM000663.1:g.19404499G>C	GRCh37
NC_000001.9:g.19277086G>C	NCBI36
NG_027669.1:g.137248C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15295C>G MANE Select	ENSP00000364403.3:p.Leu5099Val
ENST00000375224.1:c.2416C>G	ENSP00000364372.1:p.Leu806Val
ENST00000375225.7:c.520C>G	ENSP00000364373.3:p.Leu174Val
ENST00000375254.7:c.15295C>G	ENSP00000364403.3:p.Leu5099Val
ENST00000459947.5:n.3302C>G
NM_020765.2:c.15295C>G	NP_065816.2:p.Leu5099Val
XM_011541108.1:c.15448C>G	XP_011539410.1:p.Leu5150Val
XM_011541109.1:c.15445C>G	XP_011539411.1:p.Leu5149Val
XM_011541110.1:c.15445C>G	XP_011539412.1:p.Leu5149Val
XM_011541111.1:c.15445C>G	XP_011539413.1:p.Leu5149Val
XM_011541112.1:c.15433C>G	XP_011539414.1:p.Leu5145Val
XM_011541113.1:c.15430C>G	XP_011539415.1:p.Leu5144Val
XM_011541114.1:c.15430C>G	XP_011539416.1:p.Leu5144Val
XM_011541115.1:c.15424C>G	XP_011539417.1:p.Leu5142Val
XM_011541116.1:c.15415C>G	XP_011539418.1:p.Leu5139Val
XM_011541117.1:c.15364C>G	XP_011539419.1:p.Leu5122Val
XM_011541118.1:c.15361C>G	XP_011539420.1:p.Leu5121Val
XM_011541119.1:c.15328C>G	XP_011539421.1:p.Leu5110Val
XM_011541120.1:c.15325C>G	XP_011539422.1:p.Leu5109Val
XM_011541121.1:c.15292C>G	XP_011539423.1:p.Leu5098Val
XM_011541108.3:c.15562C>G	XP_011539410.2:p.Leu5188Val
XM_011541109.3:c.15559C>G	XP_011539411.2:p.Leu5187Val
XM_011541110.3:c.15559C>G	XP_011539412.2:p.Leu5187Val
XM_011541111.3:c.15559C>G	XP_011539413.2:p.Leu5187Val
XM_011541112.3:c.15547C>G	XP_011539414.2:p.Leu5183Val
XM_011541113.3:c.15544C>G	XP_011539415.2:p.Leu5182Val
XM_011541114.3:c.15544C>G	XP_011539416.2:p.Leu5182Val
XM_011541115.3:c.15538C>G	XP_011539417.2:p.Leu5180Val
XM_011541116.3:c.15529C>G	XP_011539418.2:p.Leu5177Val
XM_011541117.3:c.15478C>G	XP_011539419.2:p.Leu5160Val
XM_011541118.3:c.15475C>G	XP_011539420.2:p.Leu5159Val
XM_011541119.3:c.15442C>G	XP_011539421.2:p.Leu5148Val
XM_011541120.3:c.15439C>G	XP_011539422.2:p.Leu5147Val
XM_011541121.3:c.15406C>G	XP_011539423.2:p.Leu5136Val
XM_017000822.2:c.15541C>G	XP_016856311.2:p.Leu5181Val
XM_017000823.2:c.15514C>G	XP_016856312.2:p.Leu5172Val
XM_017000824.2:c.15460C>G	XP_016856313.2:p.Leu5154Val
XM_017000825.2:c.15445C>G	XP_016856314.2:p.Leu5149Val
XM_017000826.2:c.15442C>G	XP_016856315.2:p.Leu5148Val
XM_017000827.2:c.15427C>G	XP_016856316.2:p.Leu5143Val
XM_017000828.2:c.15403C>G	XP_016856317.2:p.Leu5135Val
XM_017000829.2:c.15355C>G	XP_016856318.2:p.Leu5119Val
XM_017000830.2:c.15304C>G	XP_016856319.2:p.Leu5102Val
NM_020765.3:c.15295C>G MANE Select	NP_065816.2:p.Leu5099Val