Canonical Allele Identifier: CA338748145

Gene: UBR4

Linked Data

• gnomAD v4: 1-19078007-G-T
• MyVariant Identifiers: chr1:g.19404501G>T (hg19) ; chr1:g.19078007G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15293C>A MANE Select	ENSP00000364403.3:p.Ala5098Asp
ENST00000375224.1:c.2414C>A	ENSP00000364372.1:p.Ala805Asp
ENST00000375225.7:c.518C>A	ENSP00000364373.3:p.Ala173Asp
ENST00000375254.7:c.15293C>A	ENSP00000364403.3:p.Ala5098Asp
ENST00000459947.5:n.3300C>A
NM_020765.2:c.15293C>A	NP_065816.2:p.Ala5098Asp
XM_011541108.1:c.15446C>A	XP_011539410.1:p.Ala5149Asp
XM_011541109.1:c.15443C>A	XP_011539411.1:p.Ala5148Asp
XM_011541110.1:c.15443C>A	XP_011539412.1:p.Ala5148Asp
XM_011541111.1:c.15443C>A	XP_011539413.1:p.Ala5148Asp
XM_011541112.1:c.15431C>A	XP_011539414.1:p.Ala5144Asp
XM_011541113.1:c.15428C>A	XP_011539415.1:p.Ala5143Asp
XM_011541114.1:c.15428C>A	XP_011539416.1:p.Ala5143Asp
XM_011541115.1:c.15422C>A	XP_011539417.1:p.Ala5141Asp
XM_011541116.1:c.15413C>A	XP_011539418.1:p.Ala5138Asp
XM_011541117.1:c.15362C>A	XP_011539419.1:p.Ala5121Asp
XM_011541118.1:c.15359C>A	XP_011539420.1:p.Ala5120Asp
XM_011541119.1:c.15326C>A	XP_011539421.1:p.Ala5109Asp
XM_011541120.1:c.15323C>A	XP_011539422.1:p.Ala5108Asp
XM_011541121.1:c.15290C>A	XP_011539423.1:p.Ala5097Asp
XM_011541108.3:c.15560C>A	XP_011539410.2:p.Ala5187Asp
XM_011541109.3:c.15557C>A	XP_011539411.2:p.Ala5186Asp
XM_011541110.3:c.15557C>A	XP_011539412.2:p.Ala5186Asp
XM_011541111.3:c.15557C>A	XP_011539413.2:p.Ala5186Asp
XM_011541112.3:c.15545C>A	XP_011539414.2:p.Ala5182Asp
XM_011541113.3:c.15542C>A	XP_011539415.2:p.Ala5181Asp
XM_011541114.3:c.15542C>A	XP_011539416.2:p.Ala5181Asp
XM_011541115.3:c.15536C>A	XP_011539417.2:p.Ala5179Asp
XM_011541116.3:c.15527C>A	XP_011539418.2:p.Ala5176Asp
XM_011541117.3:c.15476C>A	XP_011539419.2:p.Ala5159Asp
XM_011541118.3:c.15473C>A	XP_011539420.2:p.Ala5158Asp
XM_011541119.3:c.15440C>A	XP_011539421.2:p.Ala5147Asp
XM_011541120.3:c.15437C>A	XP_011539422.2:p.Ala5146Asp
XM_011541121.3:c.15404C>A	XP_011539423.2:p.Ala5135Asp
XM_017000822.2:c.15539C>A	XP_016856311.2:p.Ala5180Asp
XM_017000823.2:c.15512C>A	XP_016856312.2:p.Ala5171Asp
XM_017000824.2:c.15458C>A	XP_016856313.2:p.Ala5153Asp
XM_017000825.2:c.15443C>A	XP_016856314.2:p.Ala5148Asp
XM_017000826.2:c.15440C>A	XP_016856315.2:p.Ala5147Asp
XM_017000827.2:c.15425C>A	XP_016856316.2:p.Ala5142Asp
XM_017000828.2:c.15401C>A	XP_016856317.2:p.Ala5134Asp
XM_017000829.2:c.15353C>A	XP_016856318.2:p.Ala5118Asp
XM_017000830.2:c.15302C>A	XP_016856319.2:p.Ala5101Asp
NM_020765.3:c.15293C>A MANE Select	NP_065816.2:p.Ala5098Asp