Canonical Allele Identifier: CA338748093

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15311A>C MANE Select	ENSP00000364403.3:p.Tyr5104Ser
ENST00000375224.1:c.2432A>C	ENSP00000364372.1:p.Tyr811Ser
ENST00000375225.7:c.536A>C	ENSP00000364373.3:p.Tyr179Ser
ENST00000375254.7:c.15311A>C	ENSP00000364403.3:p.Tyr5104Ser
ENST00000459947.5:n.3318A>C
NM_020765.2:c.15311A>C	NP_065816.2:p.Tyr5104Ser
XM_011541108.1:c.15464A>C	XP_011539410.1:p.Tyr5155Ser
XM_011541109.1:c.15461A>C	XP_011539411.1:p.Tyr5154Ser
XM_011541110.1:c.15461A>C	XP_011539412.1:p.Tyr5154Ser
XM_011541111.1:c.15461A>C	XP_011539413.1:p.Tyr5154Ser
XM_011541112.1:c.15449A>C	XP_011539414.1:p.Tyr5150Ser
XM_011541113.1:c.15446A>C	XP_011539415.1:p.Tyr5149Ser
XM_011541114.1:c.15446A>C	XP_011539416.1:p.Tyr5149Ser
XM_011541115.1:c.15440A>C	XP_011539417.1:p.Tyr5147Ser
XM_011541116.1:c.15431A>C	XP_011539418.1:p.Tyr5144Ser
XM_011541117.1:c.15380A>C	XP_011539419.1:p.Tyr5127Ser
XM_011541118.1:c.15377A>C	XP_011539420.1:p.Tyr5126Ser
XM_011541119.1:c.15344A>C	XP_011539421.1:p.Tyr5115Ser
XM_011541120.1:c.15341A>C	XP_011539422.1:p.Tyr5114Ser
XM_011541121.1:c.15308A>C	XP_011539423.1:p.Tyr5103Ser
XM_011541108.3:c.15578A>C	XP_011539410.2:p.Tyr5193Ser
XM_011541109.3:c.15575A>C	XP_011539411.2:p.Tyr5192Ser
XM_011541110.3:c.15575A>C	XP_011539412.2:p.Tyr5192Ser
XM_011541111.3:c.15575A>C	XP_011539413.2:p.Tyr5192Ser
XM_011541112.3:c.15563A>C	XP_011539414.2:p.Tyr5188Ser
XM_011541113.3:c.15560A>C	XP_011539415.2:p.Tyr5187Ser
XM_011541114.3:c.15560A>C	XP_011539416.2:p.Tyr5187Ser
XM_011541115.3:c.15554A>C	XP_011539417.2:p.Tyr5185Ser
XM_011541116.3:c.15545A>C	XP_011539418.2:p.Tyr5182Ser
XM_011541117.3:c.15494A>C	XP_011539419.2:p.Tyr5165Ser
XM_011541118.3:c.15491A>C	XP_011539420.2:p.Tyr5164Ser
XM_011541119.3:c.15458A>C	XP_011539421.2:p.Tyr5153Ser
XM_011541120.3:c.15455A>C	XP_011539422.2:p.Tyr5152Ser
XM_011541121.3:c.15422A>C	XP_011539423.2:p.Tyr5141Ser
XM_017000822.2:c.15557A>C	XP_016856311.2:p.Tyr5186Ser
XM_017000823.2:c.15530A>C	XP_016856312.2:p.Tyr5177Ser
XM_017000824.2:c.15476A>C	XP_016856313.2:p.Tyr5159Ser
XM_017000825.2:c.15461A>C	XP_016856314.2:p.Tyr5154Ser
XM_017000826.2:c.15458A>C	XP_016856315.2:p.Tyr5153Ser
XM_017000827.2:c.15443A>C	XP_016856316.2:p.Tyr5148Ser
XM_017000828.2:c.15419A>C	XP_016856317.2:p.Tyr5140Ser
XM_017000829.2:c.15371A>C	XP_016856318.2:p.Tyr5124Ser
XM_017000830.2:c.15320A>C	XP_016856319.2:p.Tyr5107Ser
NM_020765.3:c.15311A>C MANE Select	NP_065816.2:p.Tyr5104Ser