Canonical Allele Identifier: CA338748164

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404508A>C (hg19) ; chr1:g.19078014A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078014A>C , CM000663.2:g.19078014A>C	GRCh38
NC_000001.10:g.19404508A>C , CM000663.1:g.19404508A>C	GRCh37
NC_000001.9:g.19277095A>C	NCBI36
NG_027669.1:g.137239T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15286T>G MANE Select	ENSP00000364403.3:p.Phe5096Val
ENST00000375224.1:c.2407T>G	ENSP00000364372.1:p.Phe803Val
ENST00000375225.7:c.511T>G	ENSP00000364373.3:p.Phe171Val
ENST00000375254.7:c.15286T>G	ENSP00000364403.3:p.Phe5096Val
ENST00000459947.5:n.3293T>G
NM_020765.2:c.15286T>G	NP_065816.2:p.Phe5096Val
XM_011541108.1:c.15439T>G	XP_011539410.1:p.Phe5147Val
XM_011541109.1:c.15436T>G	XP_011539411.1:p.Phe5146Val
XM_011541110.1:c.15436T>G	XP_011539412.1:p.Phe5146Val
XM_011541111.1:c.15436T>G	XP_011539413.1:p.Phe5146Val
XM_011541112.1:c.15424T>G	XP_011539414.1:p.Phe5142Val
XM_011541113.1:c.15421T>G	XP_011539415.1:p.Phe5141Val
XM_011541114.1:c.15421T>G	XP_011539416.1:p.Phe5141Val
XM_011541115.1:c.15415T>G	XP_011539417.1:p.Phe5139Val
XM_011541116.1:c.15406T>G	XP_011539418.1:p.Phe5136Val
XM_011541117.1:c.15355T>G	XP_011539419.1:p.Phe5119Val
XM_011541118.1:c.15352T>G	XP_011539420.1:p.Phe5118Val
XM_011541119.1:c.15319T>G	XP_011539421.1:p.Phe5107Val
XM_011541120.1:c.15316T>G	XP_011539422.1:p.Phe5106Val
XM_011541121.1:c.15283T>G	XP_011539423.1:p.Phe5095Val
XM_011541108.3:c.15553T>G	XP_011539410.2:p.Phe5185Val
XM_011541109.3:c.15550T>G	XP_011539411.2:p.Phe5184Val
XM_011541110.3:c.15550T>G	XP_011539412.2:p.Phe5184Val
XM_011541111.3:c.15550T>G	XP_011539413.2:p.Phe5184Val
XM_011541112.3:c.15538T>G	XP_011539414.2:p.Phe5180Val
XM_011541113.3:c.15535T>G	XP_011539415.2:p.Phe5179Val
XM_011541114.3:c.15535T>G	XP_011539416.2:p.Phe5179Val
XM_011541115.3:c.15529T>G	XP_011539417.2:p.Phe5177Val
XM_011541116.3:c.15520T>G	XP_011539418.2:p.Phe5174Val
XM_011541117.3:c.15469T>G	XP_011539419.2:p.Phe5157Val
XM_011541118.3:c.15466T>G	XP_011539420.2:p.Phe5156Val
XM_011541119.3:c.15433T>G	XP_011539421.2:p.Phe5145Val
XM_011541120.3:c.15430T>G	XP_011539422.2:p.Phe5144Val
XM_011541121.3:c.15397T>G	XP_011539423.2:p.Phe5133Val
XM_017000822.2:c.15532T>G	XP_016856311.2:p.Phe5178Val
XM_017000823.2:c.15505T>G	XP_016856312.2:p.Phe5169Val
XM_017000824.2:c.15451T>G	XP_016856313.2:p.Phe5151Val
XM_017000825.2:c.15436T>G	XP_016856314.2:p.Phe5146Val
XM_017000826.2:c.15433T>G	XP_016856315.2:p.Phe5145Val
XM_017000827.2:c.15418T>G	XP_016856316.2:p.Phe5140Val
XM_017000828.2:c.15394T>G	XP_016856317.2:p.Phe5132Val
XM_017000829.2:c.15346T>G	XP_016856318.2:p.Phe5116Val
XM_017000830.2:c.15295T>G	XP_016856319.2:p.Phe5099Val
NM_020765.3:c.15286T>G MANE Select	NP_065816.2:p.Phe5096Val