Canonical Allele Identifier: CA338748153

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404504C>A (hg19) ; chr1:g.19078010C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078010C>A , CM000663.2:g.19078010C>A	GRCh38
NC_000001.10:g.19404504C>A , CM000663.1:g.19404504C>A	GRCh37
NC_000001.9:g.19277091C>A	NCBI36
NG_027669.1:g.137243G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15290G>T MANE Select	ENSP00000364403.3:p.Trp5097Leu
ENST00000375224.1:c.2411G>T	ENSP00000364372.1:p.Trp804Leu
ENST00000375225.7:c.515G>T	ENSP00000364373.3:p.Trp172Leu
ENST00000375254.7:c.15290G>T	ENSP00000364403.3:p.Trp5097Leu
ENST00000459947.5:n.3297G>T
NM_020765.2:c.15290G>T	NP_065816.2:p.Trp5097Leu
XM_011541108.1:c.15443G>T	XP_011539410.1:p.Trp5148Leu
XM_011541109.1:c.15440G>T	XP_011539411.1:p.Trp5147Leu
XM_011541110.1:c.15440G>T	XP_011539412.1:p.Trp5147Leu
XM_011541111.1:c.15440G>T	XP_011539413.1:p.Trp5147Leu
XM_011541112.1:c.15428G>T	XP_011539414.1:p.Trp5143Leu
XM_011541113.1:c.15425G>T	XP_011539415.1:p.Trp5142Leu
XM_011541114.1:c.15425G>T	XP_011539416.1:p.Trp5142Leu
XM_011541115.1:c.15419G>T	XP_011539417.1:p.Trp5140Leu
XM_011541116.1:c.15410G>T	XP_011539418.1:p.Trp5137Leu
XM_011541117.1:c.15359G>T	XP_011539419.1:p.Trp5120Leu
XM_011541118.1:c.15356G>T	XP_011539420.1:p.Trp5119Leu
XM_011541119.1:c.15323G>T	XP_011539421.1:p.Trp5108Leu
XM_011541120.1:c.15320G>T	XP_011539422.1:p.Trp5107Leu
XM_011541121.1:c.15287G>T	XP_011539423.1:p.Trp5096Leu
XM_011541108.3:c.15557G>T	XP_011539410.2:p.Trp5186Leu
XM_011541109.3:c.15554G>T	XP_011539411.2:p.Trp5185Leu
XM_011541110.3:c.15554G>T	XP_011539412.2:p.Trp5185Leu
XM_011541111.3:c.15554G>T	XP_011539413.2:p.Trp5185Leu
XM_011541112.3:c.15542G>T	XP_011539414.2:p.Trp5181Leu
XM_011541113.3:c.15539G>T	XP_011539415.2:p.Trp5180Leu
XM_011541114.3:c.15539G>T	XP_011539416.2:p.Trp5180Leu
XM_011541115.3:c.15533G>T	XP_011539417.2:p.Trp5178Leu
XM_011541116.3:c.15524G>T	XP_011539418.2:p.Trp5175Leu
XM_011541117.3:c.15473G>T	XP_011539419.2:p.Trp5158Leu
XM_011541118.3:c.15470G>T	XP_011539420.2:p.Trp5157Leu
XM_011541119.3:c.15437G>T	XP_011539421.2:p.Trp5146Leu
XM_011541120.3:c.15434G>T	XP_011539422.2:p.Trp5145Leu
XM_011541121.3:c.15401G>T	XP_011539423.2:p.Trp5134Leu
XM_017000822.2:c.15536G>T	XP_016856311.2:p.Trp5179Leu
XM_017000823.2:c.15509G>T	XP_016856312.2:p.Trp5170Leu
XM_017000824.2:c.15455G>T	XP_016856313.2:p.Trp5152Leu
XM_017000825.2:c.15440G>T	XP_016856314.2:p.Trp5147Leu
XM_017000826.2:c.15437G>T	XP_016856315.2:p.Trp5146Leu
XM_017000827.2:c.15422G>T	XP_016856316.2:p.Trp5141Leu
XM_017000828.2:c.15398G>T	XP_016856317.2:p.Trp5133Leu
XM_017000829.2:c.15350G>T	XP_016856318.2:p.Trp5117Leu
XM_017000830.2:c.15299G>T	XP_016856319.2:p.Trp5100Leu
NM_020765.3:c.15290G>T MANE Select	NP_065816.2:p.Trp5097Leu