Canonical Allele Identifier: CA338748090

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404483T>A (hg19) ; chr1:g.19077989T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077989T>A , CM000663.2:g.19077989T>A	GRCh38
NC_000001.10:g.19404483T>A , CM000663.1:g.19404483T>A	GRCh37
NC_000001.9:g.19277070T>A	NCBI36
NG_027669.1:g.137264A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15311A>T MANE Select	ENSP00000364403.3:p.Tyr5104Phe
ENST00000375224.1:c.2432A>T	ENSP00000364372.1:p.Tyr811Phe
ENST00000375225.7:c.536A>T	ENSP00000364373.3:p.Tyr179Phe
ENST00000375254.7:c.15311A>T	ENSP00000364403.3:p.Tyr5104Phe
ENST00000459947.5:n.3318A>T
NM_020765.2:c.15311A>T	NP_065816.2:p.Tyr5104Phe
XM_011541108.1:c.15464A>T	XP_011539410.1:p.Tyr5155Phe
XM_011541109.1:c.15461A>T	XP_011539411.1:p.Tyr5154Phe
XM_011541110.1:c.15461A>T	XP_011539412.1:p.Tyr5154Phe
XM_011541111.1:c.15461A>T	XP_011539413.1:p.Tyr5154Phe
XM_011541112.1:c.15449A>T	XP_011539414.1:p.Tyr5150Phe
XM_011541113.1:c.15446A>T	XP_011539415.1:p.Tyr5149Phe
XM_011541114.1:c.15446A>T	XP_011539416.1:p.Tyr5149Phe
XM_011541115.1:c.15440A>T	XP_011539417.1:p.Tyr5147Phe
XM_011541116.1:c.15431A>T	XP_011539418.1:p.Tyr5144Phe
XM_011541117.1:c.15380A>T	XP_011539419.1:p.Tyr5127Phe
XM_011541118.1:c.15377A>T	XP_011539420.1:p.Tyr5126Phe
XM_011541119.1:c.15344A>T	XP_011539421.1:p.Tyr5115Phe
XM_011541120.1:c.15341A>T	XP_011539422.1:p.Tyr5114Phe
XM_011541121.1:c.15308A>T	XP_011539423.1:p.Tyr5103Phe
XM_011541108.3:c.15578A>T	XP_011539410.2:p.Tyr5193Phe
XM_011541109.3:c.15575A>T	XP_011539411.2:p.Tyr5192Phe
XM_011541110.3:c.15575A>T	XP_011539412.2:p.Tyr5192Phe
XM_011541111.3:c.15575A>T	XP_011539413.2:p.Tyr5192Phe
XM_011541112.3:c.15563A>T	XP_011539414.2:p.Tyr5188Phe
XM_011541113.3:c.15560A>T	XP_011539415.2:p.Tyr5187Phe
XM_011541114.3:c.15560A>T	XP_011539416.2:p.Tyr5187Phe
XM_011541115.3:c.15554A>T	XP_011539417.2:p.Tyr5185Phe
XM_011541116.3:c.15545A>T	XP_011539418.2:p.Tyr5182Phe
XM_011541117.3:c.15494A>T	XP_011539419.2:p.Tyr5165Phe
XM_011541118.3:c.15491A>T	XP_011539420.2:p.Tyr5164Phe
XM_011541119.3:c.15458A>T	XP_011539421.2:p.Tyr5153Phe
XM_011541120.3:c.15455A>T	XP_011539422.2:p.Tyr5152Phe
XM_011541121.3:c.15422A>T	XP_011539423.2:p.Tyr5141Phe
XM_017000822.2:c.15557A>T	XP_016856311.2:p.Tyr5186Phe
XM_017000823.2:c.15530A>T	XP_016856312.2:p.Tyr5177Phe
XM_017000824.2:c.15476A>T	XP_016856313.2:p.Tyr5159Phe
XM_017000825.2:c.15461A>T	XP_016856314.2:p.Tyr5154Phe
XM_017000826.2:c.15458A>T	XP_016856315.2:p.Tyr5153Phe
XM_017000827.2:c.15443A>T	XP_016856316.2:p.Tyr5148Phe
XM_017000828.2:c.15419A>T	XP_016856317.2:p.Tyr5140Phe
XM_017000829.2:c.15371A>T	XP_016856318.2:p.Tyr5124Phe
XM_017000830.2:c.15320A>T	XP_016856319.2:p.Tyr5107Phe
NM_020765.3:c.15311A>T MANE Select	NP_065816.2:p.Tyr5104Phe