Canonical Allele Identifier: CA416453132

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404512A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078018A>C , CM000663.2:g.19078018A>C	GRCh38
NC_000001.10:g.19404512A>C , CM000663.1:g.19404512A>C	GRCh37
NC_000001.9:g.19277099A>C	NCBI36
NG_027669.1:g.137235T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15282T>G MANE Select	ENSP00000364403.3:p.Leu5094=
ENST00000375224.1:c.2403T>G	ENSP00000364372.1:p.Leu801=
ENST00000375225.7:c.507T>G	ENSP00000364373.3:p.Leu169=
ENST00000375254.7:c.15282T>G	ENSP00000364403.3:p.Leu5094=
ENST00000459947.5:n.3289T>G
NM_020765.2:c.15282T>G	NP_065816.2:p.Leu5094=
XM_011541108.1:c.15435T>G	XP_011539410.1:p.Leu5145=
XM_011541109.1:c.15432T>G	XP_011539411.1:p.Leu5144=
XM_011541110.1:c.15432T>G	XP_011539412.1:p.Leu5144=
XM_011541111.1:c.15432T>G	XP_011539413.1:p.Leu5144=
XM_011541112.1:c.15420T>G	XP_011539414.1:p.Leu5140=
XM_011541113.1:c.15417T>G	XP_011539415.1:p.Leu5139=
XM_011541114.1:c.15417T>G	XP_011539416.1:p.Leu5139=
XM_011541115.1:c.15411T>G	XP_011539417.1:p.Leu5137=
XM_011541116.1:c.15402T>G	XP_011539418.1:p.Leu5134=
XM_011541117.1:c.15351T>G	XP_011539419.1:p.Leu5117=
XM_011541118.1:c.15348T>G	XP_011539420.1:p.Leu5116=
XM_011541119.1:c.15315T>G	XP_011539421.1:p.Leu5105=
XM_011541120.1:c.15312T>G	XP_011539422.1:p.Leu5104=
XM_011541121.1:c.15279T>G	XP_011539423.1:p.Leu5093=
XM_011541108.3:c.15549T>G	XP_011539410.2:p.Leu5183=
XM_011541109.3:c.15546T>G	XP_011539411.2:p.Leu5182=
XM_011541110.3:c.15546T>G	XP_011539412.2:p.Leu5182=
XM_011541111.3:c.15546T>G	XP_011539413.2:p.Leu5182=
XM_011541112.3:c.15534T>G	XP_011539414.2:p.Leu5178=
XM_011541113.3:c.15531T>G	XP_011539415.2:p.Leu5177=
XM_011541114.3:c.15531T>G	XP_011539416.2:p.Leu5177=
XM_011541115.3:c.15525T>G	XP_011539417.2:p.Leu5175=
XM_011541116.3:c.15516T>G	XP_011539418.2:p.Leu5172=
XM_011541117.3:c.15465T>G	XP_011539419.2:p.Leu5155=
XM_011541118.3:c.15462T>G	XP_011539420.2:p.Leu5154=
XM_011541119.3:c.15429T>G	XP_011539421.2:p.Leu5143=
XM_011541120.3:c.15426T>G	XP_011539422.2:p.Leu5142=
XM_011541121.3:c.15393T>G	XP_011539423.2:p.Leu5131=
XM_017000822.2:c.15528T>G	XP_016856311.2:p.Leu5176=
XM_017000823.2:c.15501T>G	XP_016856312.2:p.Leu5167=
XM_017000824.2:c.15447T>G	XP_016856313.2:p.Leu5149=
XM_017000825.2:c.15432T>G	XP_016856314.2:p.Leu5144=
XM_017000826.2:c.15429T>G	XP_016856315.2:p.Leu5143=
XM_017000827.2:c.15414T>G	XP_016856316.2:p.Leu5138=
XM_017000828.2:c.15390T>G	XP_016856317.2:p.Leu5130=
XM_017000829.2:c.15342T>G	XP_016856318.2:p.Leu5114=
XM_017000830.2:c.15291T>G	XP_016856319.2:p.Leu5097=
NM_020765.3:c.15282T>G MANE Select	NP_065816.2:p.Leu5094=