Canonical Allele Identifier: CA338748205

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404520A>C (hg19) ; chr1:g.19078026A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078026A>C , CM000663.2:g.19078026A>C	GRCh38
NC_000001.10:g.19404520A>C , CM000663.1:g.19404520A>C	GRCh37
NC_000001.9:g.19277107A>C	NCBI36
NG_027669.1:g.137227T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15274T>G MANE Select	ENSP00000364403.3:p.Ser5092Ala
ENST00000375224.1:c.2395T>G	ENSP00000364372.1:p.Ser799Ala
ENST00000375225.7:c.499T>G	ENSP00000364373.3:p.Ser167Ala
ENST00000375254.7:c.15274T>G	ENSP00000364403.3:p.Ser5092Ala
ENST00000459947.5:n.3281T>G
NM_020765.2:c.15274T>G	NP_065816.2:p.Ser5092Ala
XM_011541108.1:c.15427T>G	XP_011539410.1:p.Ser5143Ala
XM_011541109.1:c.15424T>G	XP_011539411.1:p.Ser5142Ala
XM_011541110.1:c.15424T>G	XP_011539412.1:p.Ser5142Ala
XM_011541111.1:c.15424T>G	XP_011539413.1:p.Ser5142Ala
XM_011541112.1:c.15412T>G	XP_011539414.1:p.Ser5138Ala
XM_011541113.1:c.15409T>G	XP_011539415.1:p.Ser5137Ala
XM_011541114.1:c.15409T>G	XP_011539416.1:p.Ser5137Ala
XM_011541115.1:c.15403T>G	XP_011539417.1:p.Ser5135Ala
XM_011541116.1:c.15394T>G	XP_011539418.1:p.Ser5132Ala
XM_011541117.1:c.15343T>G	XP_011539419.1:p.Ser5115Ala
XM_011541118.1:c.15340T>G	XP_011539420.1:p.Ser5114Ala
XM_011541119.1:c.15307T>G	XP_011539421.1:p.Ser5103Ala
XM_011541120.1:c.15304T>G	XP_011539422.1:p.Ser5102Ala
XM_011541121.1:c.15271T>G	XP_011539423.1:p.Ser5091Ala
XM_011541108.3:c.15541T>G	XP_011539410.2:p.Ser5181Ala
XM_011541109.3:c.15538T>G	XP_011539411.2:p.Ser5180Ala
XM_011541110.3:c.15538T>G	XP_011539412.2:p.Ser5180Ala
XM_011541111.3:c.15538T>G	XP_011539413.2:p.Ser5180Ala
XM_011541112.3:c.15526T>G	XP_011539414.2:p.Ser5176Ala
XM_011541113.3:c.15523T>G	XP_011539415.2:p.Ser5175Ala
XM_011541114.3:c.15523T>G	XP_011539416.2:p.Ser5175Ala
XM_011541115.3:c.15517T>G	XP_011539417.2:p.Ser5173Ala
XM_011541116.3:c.15508T>G	XP_011539418.2:p.Ser5170Ala
XM_011541117.3:c.15457T>G	XP_011539419.2:p.Ser5153Ala
XM_011541118.3:c.15454T>G	XP_011539420.2:p.Ser5152Ala
XM_011541119.3:c.15421T>G	XP_011539421.2:p.Ser5141Ala
XM_011541120.3:c.15418T>G	XP_011539422.2:p.Ser5140Ala
XM_011541121.3:c.15385T>G	XP_011539423.2:p.Ser5129Ala
XM_017000822.2:c.15520T>G	XP_016856311.2:p.Ser5174Ala
XM_017000823.2:c.15493T>G	XP_016856312.2:p.Ser5165Ala
XM_017000824.2:c.15439T>G	XP_016856313.2:p.Ser5147Ala
XM_017000825.2:c.15424T>G	XP_016856314.2:p.Ser5142Ala
XM_017000826.2:c.15421T>G	XP_016856315.2:p.Ser5141Ala
XM_017000827.2:c.15406T>G	XP_016856316.2:p.Ser5136Ala
XM_017000828.2:c.15382T>G	XP_016856317.2:p.Ser5128Ala
XM_017000829.2:c.15334T>G	XP_016856318.2:p.Ser5112Ala
XM_017000830.2:c.15283T>G	XP_016856319.2:p.Ser5095Ala
NM_020765.3:c.15274T>G MANE Select	NP_065816.2:p.Ser5092Ala