Canonical Allele Identifier: CA338748157

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404505A>G (hg19) ; chr1:g.19078011A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078011A>G , CM000663.2:g.19078011A>G	GRCh38
NC_000001.10:g.19404505A>G , CM000663.1:g.19404505A>G	GRCh37
NC_000001.9:g.19277092A>G	NCBI36
NG_027669.1:g.137242T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15289T>C MANE Select	ENSP00000364403.3:p.Trp5097Arg
ENST00000375224.1:c.2410T>C	ENSP00000364372.1:p.Trp804Arg
ENST00000375225.7:c.514T>C	ENSP00000364373.3:p.Trp172Arg
ENST00000375254.7:c.15289T>C	ENSP00000364403.3:p.Trp5097Arg
ENST00000459947.5:n.3296T>C
NM_020765.2:c.15289T>C	NP_065816.2:p.Trp5097Arg
XM_011541108.1:c.15442T>C	XP_011539410.1:p.Trp5148Arg
XM_011541109.1:c.15439T>C	XP_011539411.1:p.Trp5147Arg
XM_011541110.1:c.15439T>C	XP_011539412.1:p.Trp5147Arg
XM_011541111.1:c.15439T>C	XP_011539413.1:p.Trp5147Arg
XM_011541112.1:c.15427T>C	XP_011539414.1:p.Trp5143Arg
XM_011541113.1:c.15424T>C	XP_011539415.1:p.Trp5142Arg
XM_011541114.1:c.15424T>C	XP_011539416.1:p.Trp5142Arg
XM_011541115.1:c.15418T>C	XP_011539417.1:p.Trp5140Arg
XM_011541116.1:c.15409T>C	XP_011539418.1:p.Trp5137Arg
XM_011541117.1:c.15358T>C	XP_011539419.1:p.Trp5120Arg
XM_011541118.1:c.15355T>C	XP_011539420.1:p.Trp5119Arg
XM_011541119.1:c.15322T>C	XP_011539421.1:p.Trp5108Arg
XM_011541120.1:c.15319T>C	XP_011539422.1:p.Trp5107Arg
XM_011541121.1:c.15286T>C	XP_011539423.1:p.Trp5096Arg
XM_011541108.3:c.15556T>C	XP_011539410.2:p.Trp5186Arg
XM_011541109.3:c.15553T>C	XP_011539411.2:p.Trp5185Arg
XM_011541110.3:c.15553T>C	XP_011539412.2:p.Trp5185Arg
XM_011541111.3:c.15553T>C	XP_011539413.2:p.Trp5185Arg
XM_011541112.3:c.15541T>C	XP_011539414.2:p.Trp5181Arg
XM_011541113.3:c.15538T>C	XP_011539415.2:p.Trp5180Arg
XM_011541114.3:c.15538T>C	XP_011539416.2:p.Trp5180Arg
XM_011541115.3:c.15532T>C	XP_011539417.2:p.Trp5178Arg
XM_011541116.3:c.15523T>C	XP_011539418.2:p.Trp5175Arg
XM_011541117.3:c.15472T>C	XP_011539419.2:p.Trp5158Arg
XM_011541118.3:c.15469T>C	XP_011539420.2:p.Trp5157Arg
XM_011541119.3:c.15436T>C	XP_011539421.2:p.Trp5146Arg
XM_011541120.3:c.15433T>C	XP_011539422.2:p.Trp5145Arg
XM_011541121.3:c.15400T>C	XP_011539423.2:p.Trp5134Arg
XM_017000822.2:c.15535T>C	XP_016856311.2:p.Trp5179Arg
XM_017000823.2:c.15508T>C	XP_016856312.2:p.Trp5170Arg
XM_017000824.2:c.15454T>C	XP_016856313.2:p.Trp5152Arg
XM_017000825.2:c.15439T>C	XP_016856314.2:p.Trp5147Arg
XM_017000826.2:c.15436T>C	XP_016856315.2:p.Trp5146Arg
XM_017000827.2:c.15421T>C	XP_016856316.2:p.Trp5141Arg
XM_017000828.2:c.15397T>C	XP_016856317.2:p.Trp5133Arg
XM_017000829.2:c.15349T>C	XP_016856318.2:p.Trp5117Arg
XM_017000830.2:c.15298T>C	XP_016856319.2:p.Trp5100Arg
NM_020765.3:c.15289T>C MANE Select	NP_065816.2:p.Trp5097Arg