Canonical Allele Identifier: CA338748147

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404502C>A (hg19) ; chr1:g.19078008C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078008C>A , CM000663.2:g.19078008C>A	GRCh38
NC_000001.10:g.19404502C>A , CM000663.1:g.19404502C>A	GRCh37
NC_000001.9:g.19277089C>A	NCBI36
NG_027669.1:g.137245G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15292G>T MANE Select	ENSP00000364403.3:p.Ala5098Ser
ENST00000375224.1:c.2413G>T	ENSP00000364372.1:p.Ala805Ser
ENST00000375225.7:c.517G>T	ENSP00000364373.3:p.Ala173Ser
ENST00000375254.7:c.15292G>T	ENSP00000364403.3:p.Ala5098Ser
ENST00000459947.5:n.3299G>T
NM_020765.2:c.15292G>T	NP_065816.2:p.Ala5098Ser
XM_011541108.1:c.15445G>T	XP_011539410.1:p.Ala5149Ser
XM_011541109.1:c.15442G>T	XP_011539411.1:p.Ala5148Ser
XM_011541110.1:c.15442G>T	XP_011539412.1:p.Ala5148Ser
XM_011541111.1:c.15442G>T	XP_011539413.1:p.Ala5148Ser
XM_011541112.1:c.15430G>T	XP_011539414.1:p.Ala5144Ser
XM_011541113.1:c.15427G>T	XP_011539415.1:p.Ala5143Ser
XM_011541114.1:c.15427G>T	XP_011539416.1:p.Ala5143Ser
XM_011541115.1:c.15421G>T	XP_011539417.1:p.Ala5141Ser
XM_011541116.1:c.15412G>T	XP_011539418.1:p.Ala5138Ser
XM_011541117.1:c.15361G>T	XP_011539419.1:p.Ala5121Ser
XM_011541118.1:c.15358G>T	XP_011539420.1:p.Ala5120Ser
XM_011541119.1:c.15325G>T	XP_011539421.1:p.Ala5109Ser
XM_011541120.1:c.15322G>T	XP_011539422.1:p.Ala5108Ser
XM_011541121.1:c.15289G>T	XP_011539423.1:p.Ala5097Ser
XM_011541108.3:c.15559G>T	XP_011539410.2:p.Ala5187Ser
XM_011541109.3:c.15556G>T	XP_011539411.2:p.Ala5186Ser
XM_011541110.3:c.15556G>T	XP_011539412.2:p.Ala5186Ser
XM_011541111.3:c.15556G>T	XP_011539413.2:p.Ala5186Ser
XM_011541112.3:c.15544G>T	XP_011539414.2:p.Ala5182Ser
XM_011541113.3:c.15541G>T	XP_011539415.2:p.Ala5181Ser
XM_011541114.3:c.15541G>T	XP_011539416.2:p.Ala5181Ser
XM_011541115.3:c.15535G>T	XP_011539417.2:p.Ala5179Ser
XM_011541116.3:c.15526G>T	XP_011539418.2:p.Ala5176Ser
XM_011541117.3:c.15475G>T	XP_011539419.2:p.Ala5159Ser
XM_011541118.3:c.15472G>T	XP_011539420.2:p.Ala5158Ser
XM_011541119.3:c.15439G>T	XP_011539421.2:p.Ala5147Ser
XM_011541120.3:c.15436G>T	XP_011539422.2:p.Ala5146Ser
XM_011541121.3:c.15403G>T	XP_011539423.2:p.Ala5135Ser
XM_017000822.2:c.15538G>T	XP_016856311.2:p.Ala5180Ser
XM_017000823.2:c.15511G>T	XP_016856312.2:p.Ala5171Ser
XM_017000824.2:c.15457G>T	XP_016856313.2:p.Ala5153Ser
XM_017000825.2:c.15442G>T	XP_016856314.2:p.Ala5148Ser
XM_017000826.2:c.15439G>T	XP_016856315.2:p.Ala5147Ser
XM_017000827.2:c.15424G>T	XP_016856316.2:p.Ala5142Ser
XM_017000828.2:c.15400G>T	XP_016856317.2:p.Ala5134Ser
XM_017000829.2:c.15352G>T	XP_016856318.2:p.Ala5118Ser
XM_017000830.2:c.15301G>T	XP_016856319.2:p.Ala5101Ser
NM_020765.3:c.15292G>T MANE Select	NP_065816.2:p.Ala5098Ser