Canonical Allele Identifier: CA338748154

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15290G>C MANE Select	ENSP00000364403.3:p.Trp5097Ser
ENST00000375224.1:c.2411G>C	ENSP00000364372.1:p.Trp804Ser
ENST00000375225.7:c.515G>C	ENSP00000364373.3:p.Trp172Ser
ENST00000375254.7:c.15290G>C	ENSP00000364403.3:p.Trp5097Ser
ENST00000459947.5:n.3297G>C
NM_020765.2:c.15290G>C	NP_065816.2:p.Trp5097Ser
XM_011541108.1:c.15443G>C	XP_011539410.1:p.Trp5148Ser
XM_011541109.1:c.15440G>C	XP_011539411.1:p.Trp5147Ser
XM_011541110.1:c.15440G>C	XP_011539412.1:p.Trp5147Ser
XM_011541111.1:c.15440G>C	XP_011539413.1:p.Trp5147Ser
XM_011541112.1:c.15428G>C	XP_011539414.1:p.Trp5143Ser
XM_011541113.1:c.15425G>C	XP_011539415.1:p.Trp5142Ser
XM_011541114.1:c.15425G>C	XP_011539416.1:p.Trp5142Ser
XM_011541115.1:c.15419G>C	XP_011539417.1:p.Trp5140Ser
XM_011541116.1:c.15410G>C	XP_011539418.1:p.Trp5137Ser
XM_011541117.1:c.15359G>C	XP_011539419.1:p.Trp5120Ser
XM_011541118.1:c.15356G>C	XP_011539420.1:p.Trp5119Ser
XM_011541119.1:c.15323G>C	XP_011539421.1:p.Trp5108Ser
XM_011541120.1:c.15320G>C	XP_011539422.1:p.Trp5107Ser
XM_011541121.1:c.15287G>C	XP_011539423.1:p.Trp5096Ser
XM_011541108.3:c.15557G>C	XP_011539410.2:p.Trp5186Ser
XM_011541109.3:c.15554G>C	XP_011539411.2:p.Trp5185Ser
XM_011541110.3:c.15554G>C	XP_011539412.2:p.Trp5185Ser
XM_011541111.3:c.15554G>C	XP_011539413.2:p.Trp5185Ser
XM_011541112.3:c.15542G>C	XP_011539414.2:p.Trp5181Ser
XM_011541113.3:c.15539G>C	XP_011539415.2:p.Trp5180Ser
XM_011541114.3:c.15539G>C	XP_011539416.2:p.Trp5180Ser
XM_011541115.3:c.15533G>C	XP_011539417.2:p.Trp5178Ser
XM_011541116.3:c.15524G>C	XP_011539418.2:p.Trp5175Ser
XM_011541117.3:c.15473G>C	XP_011539419.2:p.Trp5158Ser
XM_011541118.3:c.15470G>C	XP_011539420.2:p.Trp5157Ser
XM_011541119.3:c.15437G>C	XP_011539421.2:p.Trp5146Ser
XM_011541120.3:c.15434G>C	XP_011539422.2:p.Trp5145Ser
XM_011541121.3:c.15401G>C	XP_011539423.2:p.Trp5134Ser
XM_017000822.2:c.15536G>C	XP_016856311.2:p.Trp5179Ser
XM_017000823.2:c.15509G>C	XP_016856312.2:p.Trp5170Ser
XM_017000824.2:c.15455G>C	XP_016856313.2:p.Trp5152Ser
XM_017000825.2:c.15440G>C	XP_016856314.2:p.Trp5147Ser
XM_017000826.2:c.15437G>C	XP_016856315.2:p.Trp5146Ser
XM_017000827.2:c.15422G>C	XP_016856316.2:p.Trp5141Ser
XM_017000828.2:c.15398G>C	XP_016856317.2:p.Trp5133Ser
XM_017000829.2:c.15350G>C	XP_016856318.2:p.Trp5117Ser
XM_017000830.2:c.15299G>C	XP_016856319.2:p.Trp5100Ser
NM_020765.3:c.15290G>C MANE Select	NP_065816.2:p.Trp5097Ser