Canonical Allele Identifier: CA338748134

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404495A>G (hg19) ; chr1:g.19078001A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078001A>G , CM000663.2:g.19078001A>G	GRCh38
NC_000001.10:g.19404495A>G , CM000663.1:g.19404495A>G	GRCh37
NC_000001.9:g.19277082A>G	NCBI36
NG_027669.1:g.137252T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15299T>C MANE Select	ENSP00000364403.3:p.Val5100Ala
ENST00000375224.1:c.2420T>C	ENSP00000364372.1:p.Val807Ala
ENST00000375225.7:c.524T>C	ENSP00000364373.3:p.Val175Ala
ENST00000375254.7:c.15299T>C	ENSP00000364403.3:p.Val5100Ala
ENST00000459947.5:n.3306T>C
NM_020765.2:c.15299T>C	NP_065816.2:p.Val5100Ala
XM_011541108.1:c.15452T>C	XP_011539410.1:p.Val5151Ala
XM_011541109.1:c.15449T>C	XP_011539411.1:p.Val5150Ala
XM_011541110.1:c.15449T>C	XP_011539412.1:p.Val5150Ala
XM_011541111.1:c.15449T>C	XP_011539413.1:p.Val5150Ala
XM_011541112.1:c.15437T>C	XP_011539414.1:p.Val5146Ala
XM_011541113.1:c.15434T>C	XP_011539415.1:p.Val5145Ala
XM_011541114.1:c.15434T>C	XP_011539416.1:p.Val5145Ala
XM_011541115.1:c.15428T>C	XP_011539417.1:p.Val5143Ala
XM_011541116.1:c.15419T>C	XP_011539418.1:p.Val5140Ala
XM_011541117.1:c.15368T>C	XP_011539419.1:p.Val5123Ala
XM_011541118.1:c.15365T>C	XP_011539420.1:p.Val5122Ala
XM_011541119.1:c.15332T>C	XP_011539421.1:p.Val5111Ala
XM_011541120.1:c.15329T>C	XP_011539422.1:p.Val5110Ala
XM_011541121.1:c.15296T>C	XP_011539423.1:p.Val5099Ala
XM_011541108.3:c.15566T>C	XP_011539410.2:p.Val5189Ala
XM_011541109.3:c.15563T>C	XP_011539411.2:p.Val5188Ala
XM_011541110.3:c.15563T>C	XP_011539412.2:p.Val5188Ala
XM_011541111.3:c.15563T>C	XP_011539413.2:p.Val5188Ala
XM_011541112.3:c.15551T>C	XP_011539414.2:p.Val5184Ala
XM_011541113.3:c.15548T>C	XP_011539415.2:p.Val5183Ala
XM_011541114.3:c.15548T>C	XP_011539416.2:p.Val5183Ala
XM_011541115.3:c.15542T>C	XP_011539417.2:p.Val5181Ala
XM_011541116.3:c.15533T>C	XP_011539418.2:p.Val5178Ala
XM_011541117.3:c.15482T>C	XP_011539419.2:p.Val5161Ala
XM_011541118.3:c.15479T>C	XP_011539420.2:p.Val5160Ala
XM_011541119.3:c.15446T>C	XP_011539421.2:p.Val5149Ala
XM_011541120.3:c.15443T>C	XP_011539422.2:p.Val5148Ala
XM_011541121.3:c.15410T>C	XP_011539423.2:p.Val5137Ala
XM_017000822.2:c.15545T>C	XP_016856311.2:p.Val5182Ala
XM_017000823.2:c.15518T>C	XP_016856312.2:p.Val5173Ala
XM_017000824.2:c.15464T>C	XP_016856313.2:p.Val5155Ala
XM_017000825.2:c.15449T>C	XP_016856314.2:p.Val5150Ala
XM_017000826.2:c.15446T>C	XP_016856315.2:p.Val5149Ala
XM_017000827.2:c.15431T>C	XP_016856316.2:p.Val5144Ala
XM_017000828.2:c.15407T>C	XP_016856317.2:p.Val5136Ala
XM_017000829.2:c.15359T>C	XP_016856318.2:p.Val5120Ala
XM_017000830.2:c.15308T>C	XP_016856319.2:p.Val5103Ala
NM_020765.3:c.15299T>C MANE Select	NP_065816.2:p.Val5100Ala