Canonical Allele Identifier: CA416453155

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404527A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078033A>C , CM000663.2:g.19078033A>C	GRCh38
NC_000001.10:g.19404527A>C , CM000663.1:g.19404527A>C	GRCh37
NC_000001.9:g.19277114A>C	NCBI36
NG_027669.1:g.137220T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15267T>G MANE Select	ENSP00000364403.3:p.Ala5089=
ENST00000375224.1:c.2388T>G	ENSP00000364372.1:p.Ala796=
ENST00000375225.7:c.492T>G	ENSP00000364373.3:p.Ala164=
ENST00000375254.7:c.15267T>G	ENSP00000364403.3:p.Ala5089=
ENST00000459947.5:n.3274T>G
NM_020765.2:c.15267T>G	NP_065816.2:p.Ala5089=
XM_011541108.1:c.15420T>G	XP_011539410.1:p.Ala5140=
XM_011541109.1:c.15417T>G	XP_011539411.1:p.Ala5139=
XM_011541110.1:c.15417T>G	XP_011539412.1:p.Ala5139=
XM_011541111.1:c.15417T>G	XP_011539413.1:p.Ala5139=
XM_011541112.1:c.15405T>G	XP_011539414.1:p.Ala5135=
XM_011541113.1:c.15402T>G	XP_011539415.1:p.Ala5134=
XM_011541114.1:c.15402T>G	XP_011539416.1:p.Ala5134=
XM_011541115.1:c.15396T>G	XP_011539417.1:p.Ala5132=
XM_011541116.1:c.15387T>G	XP_011539418.1:p.Ala5129=
XM_011541117.1:c.15336T>G	XP_011539419.1:p.Ala5112=
XM_011541118.1:c.15333T>G	XP_011539420.1:p.Ala5111=
XM_011541119.1:c.15300T>G	XP_011539421.1:p.Ala5100=
XM_011541120.1:c.15297T>G	XP_011539422.1:p.Ala5099=
XM_011541121.1:c.15264T>G	XP_011539423.1:p.Ala5088=
XM_011541108.3:c.15534T>G	XP_011539410.2:p.Ala5178=
XM_011541109.3:c.15531T>G	XP_011539411.2:p.Ala5177=
XM_011541110.3:c.15531T>G	XP_011539412.2:p.Ala5177=
XM_011541111.3:c.15531T>G	XP_011539413.2:p.Ala5177=
XM_011541112.3:c.15519T>G	XP_011539414.2:p.Ala5173=
XM_011541113.3:c.15516T>G	XP_011539415.2:p.Ala5172=
XM_011541114.3:c.15516T>G	XP_011539416.2:p.Ala5172=
XM_011541115.3:c.15510T>G	XP_011539417.2:p.Ala5170=
XM_011541116.3:c.15501T>G	XP_011539418.2:p.Ala5167=
XM_011541117.3:c.15450T>G	XP_011539419.2:p.Ala5150=
XM_011541118.3:c.15447T>G	XP_011539420.2:p.Ala5149=
XM_011541119.3:c.15414T>G	XP_011539421.2:p.Ala5138=
XM_011541120.3:c.15411T>G	XP_011539422.2:p.Ala5137=
XM_011541121.3:c.15378T>G	XP_011539423.2:p.Ala5126=
XM_017000822.2:c.15513T>G	XP_016856311.2:p.Ala5171=
XM_017000823.2:c.15486T>G	XP_016856312.2:p.Ala5162=
XM_017000824.2:c.15432T>G	XP_016856313.2:p.Ala5144=
XM_017000825.2:c.15417T>G	XP_016856314.2:p.Ala5139=
XM_017000826.2:c.15414T>G	XP_016856315.2:p.Ala5138=
XM_017000827.2:c.15399T>G	XP_016856316.2:p.Ala5133=
XM_017000828.2:c.15375T>G	XP_016856317.2:p.Ala5125=
XM_017000829.2:c.15327T>G	XP_016856318.2:p.Ala5109=
XM_017000830.2:c.15276T>G	XP_016856319.2:p.Ala5092=
NM_020765.3:c.15267T>G MANE Select	NP_065816.2:p.Ala5089=