Canonical Allele Identifier: CA416453151

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404521A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078027A>C , CM000663.2:g.19078027A>C	GRCh38
NC_000001.10:g.19404521A>C , CM000663.1:g.19404521A>C	GRCh37
NC_000001.9:g.19277108A>C	NCBI36
NG_027669.1:g.137226T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15273T>G MANE Select	ENSP00000364403.3:p.Arg5091=
ENST00000375224.1:c.2394T>G	ENSP00000364372.1:p.Arg798=
ENST00000375225.7:c.498T>G	ENSP00000364373.3:p.Arg166=
ENST00000375254.7:c.15273T>G	ENSP00000364403.3:p.Arg5091=
ENST00000459947.5:n.3280T>G
NM_020765.2:c.15273T>G	NP_065816.2:p.Arg5091=
XM_011541108.1:c.15426T>G	XP_011539410.1:p.Arg5142=
XM_011541109.1:c.15423T>G	XP_011539411.1:p.Arg5141=
XM_011541110.1:c.15423T>G	XP_011539412.1:p.Arg5141=
XM_011541111.1:c.15423T>G	XP_011539413.1:p.Arg5141=
XM_011541112.1:c.15411T>G	XP_011539414.1:p.Arg5137=
XM_011541113.1:c.15408T>G	XP_011539415.1:p.Arg5136=
XM_011541114.1:c.15408T>G	XP_011539416.1:p.Arg5136=
XM_011541115.1:c.15402T>G	XP_011539417.1:p.Arg5134=
XM_011541116.1:c.15393T>G	XP_011539418.1:p.Arg5131=
XM_011541117.1:c.15342T>G	XP_011539419.1:p.Arg5114=
XM_011541118.1:c.15339T>G	XP_011539420.1:p.Arg5113=
XM_011541119.1:c.15306T>G	XP_011539421.1:p.Arg5102=
XM_011541120.1:c.15303T>G	XP_011539422.1:p.Arg5101=
XM_011541121.1:c.15270T>G	XP_011539423.1:p.Arg5090=
XM_011541108.3:c.15540T>G	XP_011539410.2:p.Arg5180=
XM_011541109.3:c.15537T>G	XP_011539411.2:p.Arg5179=
XM_011541110.3:c.15537T>G	XP_011539412.2:p.Arg5179=
XM_011541111.3:c.15537T>G	XP_011539413.2:p.Arg5179=
XM_011541112.3:c.15525T>G	XP_011539414.2:p.Arg5175=
XM_011541113.3:c.15522T>G	XP_011539415.2:p.Arg5174=
XM_011541114.3:c.15522T>G	XP_011539416.2:p.Arg5174=
XM_011541115.3:c.15516T>G	XP_011539417.2:p.Arg5172=
XM_011541116.3:c.15507T>G	XP_011539418.2:p.Arg5169=
XM_011541117.3:c.15456T>G	XP_011539419.2:p.Arg5152=
XM_011541118.3:c.15453T>G	XP_011539420.2:p.Arg5151=
XM_011541119.3:c.15420T>G	XP_011539421.2:p.Arg5140=
XM_011541120.3:c.15417T>G	XP_011539422.2:p.Arg5139=
XM_011541121.3:c.15384T>G	XP_011539423.2:p.Arg5128=
XM_017000822.2:c.15519T>G	XP_016856311.2:p.Arg5173=
XM_017000823.2:c.15492T>G	XP_016856312.2:p.Arg5164=
XM_017000824.2:c.15438T>G	XP_016856313.2:p.Arg5146=
XM_017000825.2:c.15423T>G	XP_016856314.2:p.Arg5141=
XM_017000826.2:c.15420T>G	XP_016856315.2:p.Arg5140=
XM_017000827.2:c.15405T>G	XP_016856316.2:p.Arg5135=
XM_017000828.2:c.15381T>G	XP_016856317.2:p.Arg5127=
XM_017000829.2:c.15333T>G	XP_016856318.2:p.Arg5111=
XM_017000830.2:c.15282T>G	XP_016856319.2:p.Arg5094=
NM_020765.3:c.15273T>G MANE Select	NP_065816.2:p.Arg5091=