Canonical Allele Identifier: CA416453175
Gene: UBR4 HGNC NCBI

Linked Data

gnomAD v4: 1-19078063-C-T
MyVariant Identifiers: chr1:g.19404557C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19078063C>T , CM000663.2:g.19078063C>T GRCh38
NC_000001.10:g.19404557C>T , CM000663.1:g.19404557C>T GRCh37
NC_000001.9:g.19277144C>T NCBI36
NG_027669.1:g.137190G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15237G>A MANE Select ENSP00000364403.3:p.Leu5079=
ENST00000375224.1:c.2358G>A ENSP00000364372.1:p.Leu786=
ENST00000375225.7:c.462G>A ENSP00000364373.3:p.Leu154=
ENST00000375254.7:c.15237G>A ENSP00000364403.3:p.Leu5079=
ENST00000459947.5:n.3244G>A
NM_020765.2:c.15237G>A NP_065816.2:p.Leu5079=
XM_011541108.1:c.15390G>A XP_011539410.1:p.Leu5130=
XM_011541109.1:c.15387G>A XP_011539411.1:p.Leu5129=
XM_011541110.1:c.15387G>A XP_011539412.1:p.Leu5129=
XM_011541111.1:c.15387G>A XP_011539413.1:p.Leu5129=
XM_011541112.1:c.15375G>A XP_011539414.1:p.Leu5125=
XM_011541113.1:c.15372G>A XP_011539415.1:p.Leu5124=
XM_011541114.1:c.15372G>A XP_011539416.1:p.Leu5124=
XM_011541115.1:c.15366G>A XP_011539417.1:p.Leu5122=
XM_011541116.1:c.15357G>A XP_011539418.1:p.Leu5119=
XM_011541117.1:c.15306G>A XP_011539419.1:p.Leu5102=
XM_011541118.1:c.15303G>A XP_011539420.1:p.Leu5101=
XM_011541119.1:c.15270G>A XP_011539421.1:p.Leu5090=
XM_011541120.1:c.15267G>A XP_011539422.1:p.Leu5089=
XM_011541121.1:c.15234G>A XP_011539423.1:p.Leu5078=
XM_011541108.3:c.15504G>A XP_011539410.2:p.Leu5168=
XM_011541109.3:c.15501G>A XP_011539411.2:p.Leu5167=
XM_011541110.3:c.15501G>A XP_011539412.2:p.Leu5167=
XM_011541111.3:c.15501G>A XP_011539413.2:p.Leu5167=
XM_011541112.3:c.15489G>A XP_011539414.2:p.Leu5163=
XM_011541113.3:c.15486G>A XP_011539415.2:p.Leu5162=
XM_011541114.3:c.15486G>A XP_011539416.2:p.Leu5162=
XM_011541115.3:c.15480G>A XP_011539417.2:p.Leu5160=
XM_011541116.3:c.15471G>A XP_011539418.2:p.Leu5157=
XM_011541117.3:c.15420G>A XP_011539419.2:p.Leu5140=
XM_011541118.3:c.15417G>A XP_011539420.2:p.Leu5139=
XM_011541119.3:c.15384G>A XP_011539421.2:p.Leu5128=
XM_011541120.3:c.15381G>A XP_011539422.2:p.Leu5127=
XM_011541121.3:c.15348G>A XP_011539423.2:p.Leu5116=
XM_017000822.2:c.15483G>A XP_016856311.2:p.Leu5161=
XM_017000823.2:c.15456G>A XP_016856312.2:p.Leu5152=
XM_017000824.2:c.15402G>A XP_016856313.2:p.Leu5134=
XM_017000825.2:c.15387G>A XP_016856314.2:p.Leu5129=
XM_017000826.2:c.15384G>A XP_016856315.2:p.Leu5128=
XM_017000827.2:c.15369G>A XP_016856316.2:p.Leu5123=
XM_017000828.2:c.15345G>A XP_016856317.2:p.Leu5115=
XM_017000829.2:c.15297G>A XP_016856318.2:p.Leu5099=
XM_017000830.2:c.15246G>A XP_016856319.2:p.Leu5082=
NM_020765.3:c.15237G>A MANE Select NP_065816.2:p.Leu5079=