Canonical Allele Identifier: CA1156956192
Gene: UBR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.19078333_19078334delinsCG , CM000663.2:g.19078333_19078334delinsCG GRCh38
NC_000001.10:g.19404827_19404828delinsCG , CM000663.1:g.19404827_19404828delinsCG GRCh37
NC_000001.9:g.19277414_19277415delinsCG NCBI36
NG_027669.1:g.136919_136920delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000375254.8:c.15234-268_15234-267delinsCG MANE Select ENSP00000364403.3:n.15234-268_15234-267delinsCG
ENST00000375224.1:c.2355-268_2355-267delinsCG ENSP00000364372.1:n.2355-268_2355-267delinsCG
ENST00000375225.7:c.459-268_459-267delinsCG ENSP00000364373.3:n.459-268_459-267delinsCG
ENST00000375254.7:c.15234-268_15234-267delinsCG ENSP00000364403.3:n.15234-268_15234-267delinsCG
ENST00000459947.5:n.2973_2974delinsCG
NM_020765.2:c.15234-268_15234-267delinsCG NP_065816.2:n.15234-268_15234-267delinsCG
XM_011541108.1:c.15387-268_15387-267delinsCG XP_011539410.1:n.15387-268_15387-267delinsCG
XM_011541109.1:c.15384-268_15384-267delinsCG XP_011539411.1:n.15384-268_15384-267delinsCG
XM_011541110.1:c.15384-268_15384-267delinsCG XP_011539412.1:n.15384-268_15384-267delinsCG
XM_011541111.1:c.15384-268_15384-267delinsCG XP_011539413.1:n.15384-268_15384-267delinsCG
XM_011541112.1:c.15372-268_15372-267delinsCG XP_011539414.1:n.15372-268_15372-267delinsCG
XM_011541113.1:c.15369-268_15369-267delinsCG XP_011539415.1:n.15369-268_15369-267delinsCG
XM_011541114.1:c.15369-268_15369-267delinsCG XP_011539416.1:n.15369-268_15369-267delinsCG
XM_011541115.1:c.15363-268_15363-267delinsCG XP_011539417.1:n.15363-268_15363-267delinsCG
XM_011541116.1:c.15354-268_15354-267delinsCG XP_011539418.1:n.15354-268_15354-267delinsCG
XM_011541117.1:c.15303-268_15303-267delinsCG XP_011539419.1:n.15303-268_15303-267delinsCG
XM_011541118.1:c.15300-268_15300-267delinsCG XP_011539420.1:n.15300-268_15300-267delinsCG
XM_011541119.1:c.15267-268_15267-267delinsCG XP_011539421.1:n.15267-268_15267-267delinsCG
XM_011541120.1:c.15264-268_15264-267delinsCG XP_011539422.1:n.15264-268_15264-267delinsCG
XM_011541121.1:c.15231-268_15231-267delinsCG XP_011539423.1:n.15231-268_15231-267delinsCG
XM_011541108.3:c.15501-268_15501-267delinsCG XP_011539410.2:n.15501-268_15501-267delinsCG
XM_011541109.3:c.15498-268_15498-267delinsCG XP_011539411.2:n.15498-268_15498-267delinsCG
XM_011541110.3:c.15498-268_15498-267delinsCG XP_011539412.2:n.15498-268_15498-267delinsCG
XM_011541111.3:c.15498-268_15498-267delinsCG XP_011539413.2:n.15498-268_15498-267delinsCG
XM_011541112.3:c.15486-268_15486-267delinsCG XP_011539414.2:n.15486-268_15486-267delinsCG
XM_011541113.3:c.15483-268_15483-267delinsCG XP_011539415.2:n.15483-268_15483-267delinsCG
XM_011541114.3:c.15483-268_15483-267delinsCG XP_011539416.2:n.15483-268_15483-267delinsCG
XM_011541115.3:c.15477-268_15477-267delinsCG XP_011539417.2:n.15477-268_15477-267delinsCG
XM_011541116.3:c.15468-268_15468-267delinsCG XP_011539418.2:n.15468-268_15468-267delinsCG
XM_011541117.3:c.15417-268_15417-267delinsCG XP_011539419.2:n.15417-268_15417-267delinsCG
XM_011541118.3:c.15414-268_15414-267delinsCG XP_011539420.2:n.15414-268_15414-267delinsCG
XM_011541119.3:c.15381-268_15381-267delinsCG XP_011539421.2:n.15381-268_15381-267delinsCG
XM_011541120.3:c.15378-268_15378-267delinsCG XP_011539422.2:n.15378-268_15378-267delinsCG
XM_011541121.3:c.15345-268_15345-267delinsCG XP_011539423.2:n.15345-268_15345-267delinsCG
XM_017000822.2:c.15480-268_15480-267delinsCG XP_016856311.2:n.15480-268_15480-267delinsCG
XM_017000823.2:c.15453-268_15453-267delinsCG XP_016856312.2:n.15453-268_15453-267delinsCG
XM_017000824.2:c.15399-268_15399-267delinsCG XP_016856313.2:n.15399-268_15399-267delinsCG
XM_017000825.2:c.15384-268_15384-267delinsCG XP_016856314.2:n.15384-268_15384-267delinsCG
XM_017000826.2:c.15381-268_15381-267delinsCG XP_016856315.2:n.15381-268_15381-267delinsCG
XM_017000827.2:c.15366-268_15366-267delinsCG XP_016856316.2:n.15366-268_15366-267delinsCG
XM_017000828.2:c.15342-268_15342-267delinsCG XP_016856317.2:n.15342-268_15342-267delinsCG
XM_017000829.2:c.15294-268_15294-267delinsCG XP_016856318.2:n.15294-268_15294-267delinsCG
XM_017000830.2:c.15243-268_15243-267delinsCG XP_016856319.2:n.15243-268_15243-267delinsCG
NM_020765.3:c.15234-268_15234-267delinsCG MANE Select NP_065816.2:n.15234-268_15234-267delinsCG