Canonical Allele Identifier: CA338748146

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404501G>A (hg19) ; chr1:g.19078007G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078007G>A , CM000663.2:g.19078007G>A	GRCh38
NC_000001.10:g.19404501G>A , CM000663.1:g.19404501G>A	GRCh37
NC_000001.9:g.19277088G>A	NCBI36
NG_027669.1:g.137246C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15293C>T MANE Select	ENSP00000364403.3:p.Ala5098Val
ENST00000375224.1:c.2414C>T	ENSP00000364372.1:p.Ala805Val
ENST00000375225.7:c.518C>T	ENSP00000364373.3:p.Ala173Val
ENST00000375254.7:c.15293C>T	ENSP00000364403.3:p.Ala5098Val
ENST00000459947.5:n.3300C>T
NM_020765.2:c.15293C>T	NP_065816.2:p.Ala5098Val
XM_011541108.1:c.15446C>T	XP_011539410.1:p.Ala5149Val
XM_011541109.1:c.15443C>T	XP_011539411.1:p.Ala5148Val
XM_011541110.1:c.15443C>T	XP_011539412.1:p.Ala5148Val
XM_011541111.1:c.15443C>T	XP_011539413.1:p.Ala5148Val
XM_011541112.1:c.15431C>T	XP_011539414.1:p.Ala5144Val
XM_011541113.1:c.15428C>T	XP_011539415.1:p.Ala5143Val
XM_011541114.1:c.15428C>T	XP_011539416.1:p.Ala5143Val
XM_011541115.1:c.15422C>T	XP_011539417.1:p.Ala5141Val
XM_011541116.1:c.15413C>T	XP_011539418.1:p.Ala5138Val
XM_011541117.1:c.15362C>T	XP_011539419.1:p.Ala5121Val
XM_011541118.1:c.15359C>T	XP_011539420.1:p.Ala5120Val
XM_011541119.1:c.15326C>T	XP_011539421.1:p.Ala5109Val
XM_011541120.1:c.15323C>T	XP_011539422.1:p.Ala5108Val
XM_011541121.1:c.15290C>T	XP_011539423.1:p.Ala5097Val
XM_011541108.3:c.15560C>T	XP_011539410.2:p.Ala5187Val
XM_011541109.3:c.15557C>T	XP_011539411.2:p.Ala5186Val
XM_011541110.3:c.15557C>T	XP_011539412.2:p.Ala5186Val
XM_011541111.3:c.15557C>T	XP_011539413.2:p.Ala5186Val
XM_011541112.3:c.15545C>T	XP_011539414.2:p.Ala5182Val
XM_011541113.3:c.15542C>T	XP_011539415.2:p.Ala5181Val
XM_011541114.3:c.15542C>T	XP_011539416.2:p.Ala5181Val
XM_011541115.3:c.15536C>T	XP_011539417.2:p.Ala5179Val
XM_011541116.3:c.15527C>T	XP_011539418.2:p.Ala5176Val
XM_011541117.3:c.15476C>T	XP_011539419.2:p.Ala5159Val
XM_011541118.3:c.15473C>T	XP_011539420.2:p.Ala5158Val
XM_011541119.3:c.15440C>T	XP_011539421.2:p.Ala5147Val
XM_011541120.3:c.15437C>T	XP_011539422.2:p.Ala5146Val
XM_011541121.3:c.15404C>T	XP_011539423.2:p.Ala5135Val
XM_017000822.2:c.15539C>T	XP_016856311.2:p.Ala5180Val
XM_017000823.2:c.15512C>T	XP_016856312.2:p.Ala5171Val
XM_017000824.2:c.15458C>T	XP_016856313.2:p.Ala5153Val
XM_017000825.2:c.15443C>T	XP_016856314.2:p.Ala5148Val
XM_017000826.2:c.15440C>T	XP_016856315.2:p.Ala5147Val
XM_017000827.2:c.15425C>T	XP_016856316.2:p.Ala5142Val
XM_017000828.2:c.15401C>T	XP_016856317.2:p.Ala5134Val
XM_017000829.2:c.15353C>T	XP_016856318.2:p.Ala5118Val
XM_017000830.2:c.15302C>T	XP_016856319.2:p.Ala5101Val
NM_020765.3:c.15293C>T MANE Select	NP_065816.2:p.Ala5098Val