Canonical Allele Identifier: CA338748162

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404507A>G (hg19) ; chr1:g.19078013A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078013A>G , CM000663.2:g.19078013A>G	GRCh38
NC_000001.10:g.19404507A>G , CM000663.1:g.19404507A>G	GRCh37
NC_000001.9:g.19277094A>G	NCBI36
NG_027669.1:g.137240T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15287T>C MANE Select	ENSP00000364403.3:p.Phe5096Ser
ENST00000375224.1:c.2408T>C	ENSP00000364372.1:p.Phe803Ser
ENST00000375225.7:c.512T>C	ENSP00000364373.3:p.Phe171Ser
ENST00000375254.7:c.15287T>C	ENSP00000364403.3:p.Phe5096Ser
ENST00000459947.5:n.3294T>C
NM_020765.2:c.15287T>C	NP_065816.2:p.Phe5096Ser
XM_011541108.1:c.15440T>C	XP_011539410.1:p.Phe5147Ser
XM_011541109.1:c.15437T>C	XP_011539411.1:p.Phe5146Ser
XM_011541110.1:c.15437T>C	XP_011539412.1:p.Phe5146Ser
XM_011541111.1:c.15437T>C	XP_011539413.1:p.Phe5146Ser
XM_011541112.1:c.15425T>C	XP_011539414.1:p.Phe5142Ser
XM_011541113.1:c.15422T>C	XP_011539415.1:p.Phe5141Ser
XM_011541114.1:c.15422T>C	XP_011539416.1:p.Phe5141Ser
XM_011541115.1:c.15416T>C	XP_011539417.1:p.Phe5139Ser
XM_011541116.1:c.15407T>C	XP_011539418.1:p.Phe5136Ser
XM_011541117.1:c.15356T>C	XP_011539419.1:p.Phe5119Ser
XM_011541118.1:c.15353T>C	XP_011539420.1:p.Phe5118Ser
XM_011541119.1:c.15320T>C	XP_011539421.1:p.Phe5107Ser
XM_011541120.1:c.15317T>C	XP_011539422.1:p.Phe5106Ser
XM_011541121.1:c.15284T>C	XP_011539423.1:p.Phe5095Ser
XM_011541108.3:c.15554T>C	XP_011539410.2:p.Phe5185Ser
XM_011541109.3:c.15551T>C	XP_011539411.2:p.Phe5184Ser
XM_011541110.3:c.15551T>C	XP_011539412.2:p.Phe5184Ser
XM_011541111.3:c.15551T>C	XP_011539413.2:p.Phe5184Ser
XM_011541112.3:c.15539T>C	XP_011539414.2:p.Phe5180Ser
XM_011541113.3:c.15536T>C	XP_011539415.2:p.Phe5179Ser
XM_011541114.3:c.15536T>C	XP_011539416.2:p.Phe5179Ser
XM_011541115.3:c.15530T>C	XP_011539417.2:p.Phe5177Ser
XM_011541116.3:c.15521T>C	XP_011539418.2:p.Phe5174Ser
XM_011541117.3:c.15470T>C	XP_011539419.2:p.Phe5157Ser
XM_011541118.3:c.15467T>C	XP_011539420.2:p.Phe5156Ser
XM_011541119.3:c.15434T>C	XP_011539421.2:p.Phe5145Ser
XM_011541120.3:c.15431T>C	XP_011539422.2:p.Phe5144Ser
XM_011541121.3:c.15398T>C	XP_011539423.2:p.Phe5133Ser
XM_017000822.2:c.15533T>C	XP_016856311.2:p.Phe5178Ser
XM_017000823.2:c.15506T>C	XP_016856312.2:p.Phe5169Ser
XM_017000824.2:c.15452T>C	XP_016856313.2:p.Phe5151Ser
XM_017000825.2:c.15437T>C	XP_016856314.2:p.Phe5146Ser
XM_017000826.2:c.15434T>C	XP_016856315.2:p.Phe5145Ser
XM_017000827.2:c.15419T>C	XP_016856316.2:p.Phe5140Ser
XM_017000828.2:c.15395T>C	XP_016856317.2:p.Phe5132Ser
XM_017000829.2:c.15347T>C	XP_016856318.2:p.Phe5116Ser
XM_017000830.2:c.15296T>C	XP_016856319.2:p.Phe5099Ser
NM_020765.3:c.15287T>C MANE Select	NP_065816.2:p.Phe5096Ser