Canonical Allele Identifier: CA338748203

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404519G>T (hg19) ; chr1:g.19078025G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078025G>T , CM000663.2:g.19078025G>T	GRCh38
NC_000001.10:g.19404519G>T , CM000663.1:g.19404519G>T	GRCh37
NC_000001.9:g.19277106G>T	NCBI36
NG_027669.1:g.137228C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15275C>A MANE Select	ENSP00000364403.3:p.Ser5092Tyr
ENST00000375224.1:c.2396C>A	ENSP00000364372.1:p.Ser799Tyr
ENST00000375225.7:c.500C>A	ENSP00000364373.3:p.Ser167Tyr
ENST00000375254.7:c.15275C>A	ENSP00000364403.3:p.Ser5092Tyr
ENST00000459947.5:n.3282C>A
NM_020765.2:c.15275C>A	NP_065816.2:p.Ser5092Tyr
XM_011541108.1:c.15428C>A	XP_011539410.1:p.Ser5143Tyr
XM_011541109.1:c.15425C>A	XP_011539411.1:p.Ser5142Tyr
XM_011541110.1:c.15425C>A	XP_011539412.1:p.Ser5142Tyr
XM_011541111.1:c.15425C>A	XP_011539413.1:p.Ser5142Tyr
XM_011541112.1:c.15413C>A	XP_011539414.1:p.Ser5138Tyr
XM_011541113.1:c.15410C>A	XP_011539415.1:p.Ser5137Tyr
XM_011541114.1:c.15410C>A	XP_011539416.1:p.Ser5137Tyr
XM_011541115.1:c.15404C>A	XP_011539417.1:p.Ser5135Tyr
XM_011541116.1:c.15395C>A	XP_011539418.1:p.Ser5132Tyr
XM_011541117.1:c.15344C>A	XP_011539419.1:p.Ser5115Tyr
XM_011541118.1:c.15341C>A	XP_011539420.1:p.Ser5114Tyr
XM_011541119.1:c.15308C>A	XP_011539421.1:p.Ser5103Tyr
XM_011541120.1:c.15305C>A	XP_011539422.1:p.Ser5102Tyr
XM_011541121.1:c.15272C>A	XP_011539423.1:p.Ser5091Tyr
XM_011541108.3:c.15542C>A	XP_011539410.2:p.Ser5181Tyr
XM_011541109.3:c.15539C>A	XP_011539411.2:p.Ser5180Tyr
XM_011541110.3:c.15539C>A	XP_011539412.2:p.Ser5180Tyr
XM_011541111.3:c.15539C>A	XP_011539413.2:p.Ser5180Tyr
XM_011541112.3:c.15527C>A	XP_011539414.2:p.Ser5176Tyr
XM_011541113.3:c.15524C>A	XP_011539415.2:p.Ser5175Tyr
XM_011541114.3:c.15524C>A	XP_011539416.2:p.Ser5175Tyr
XM_011541115.3:c.15518C>A	XP_011539417.2:p.Ser5173Tyr
XM_011541116.3:c.15509C>A	XP_011539418.2:p.Ser5170Tyr
XM_011541117.3:c.15458C>A	XP_011539419.2:p.Ser5153Tyr
XM_011541118.3:c.15455C>A	XP_011539420.2:p.Ser5152Tyr
XM_011541119.3:c.15422C>A	XP_011539421.2:p.Ser5141Tyr
XM_011541120.3:c.15419C>A	XP_011539422.2:p.Ser5140Tyr
XM_011541121.3:c.15386C>A	XP_011539423.2:p.Ser5129Tyr
XM_017000822.2:c.15521C>A	XP_016856311.2:p.Ser5174Tyr
XM_017000823.2:c.15494C>A	XP_016856312.2:p.Ser5165Tyr
XM_017000824.2:c.15440C>A	XP_016856313.2:p.Ser5147Tyr
XM_017000825.2:c.15425C>A	XP_016856314.2:p.Ser5142Tyr
XM_017000826.2:c.15422C>A	XP_016856315.2:p.Ser5141Tyr
XM_017000827.2:c.15407C>A	XP_016856316.2:p.Ser5136Tyr
XM_017000828.2:c.15383C>A	XP_016856317.2:p.Ser5128Tyr
XM_017000829.2:c.15335C>A	XP_016856318.2:p.Ser5112Tyr
XM_017000830.2:c.15284C>A	XP_016856319.2:p.Ser5095Tyr
NM_020765.3:c.15275C>A MANE Select	NP_065816.2:p.Ser5092Tyr