Canonical Allele Identifier: CA2643751599

Gene: UBR4

Linked Data

• gnomAD v4: 1-19078329-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078329G>A , CM000663.2:g.19078329G>A	GRCh38
NC_000001.10:g.19404823G>A , CM000663.1:g.19404823G>A	GRCh37
NC_000001.9:g.19277410G>A	NCBI36
NG_027669.1:g.136924C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15234-263C>T MANE Select	ENSP00000364403.3:n.15234-263C>T
ENST00000375224.1:c.2355-263C>T	ENSP00000364372.1:n.2355-263C>T
ENST00000375225.7:c.459-263C>T	ENSP00000364373.3:n.459-263C>T
ENST00000375254.7:c.15234-263C>T	ENSP00000364403.3:n.15234-263C>T
ENST00000459947.5:n.2978C>T
NM_020765.2:c.15234-263C>T	NP_065816.2:n.15234-263C>T
XM_011541108.1:c.15387-263C>T	XP_011539410.1:n.15387-263C>T
XM_011541109.1:c.15384-263C>T	XP_011539411.1:n.15384-263C>T
XM_011541110.1:c.15384-263C>T	XP_011539412.1:n.15384-263C>T
XM_011541111.1:c.15384-263C>T	XP_011539413.1:n.15384-263C>T
XM_011541112.1:c.15372-263C>T	XP_011539414.1:n.15372-263C>T
XM_011541113.1:c.15369-263C>T	XP_011539415.1:n.15369-263C>T
XM_011541114.1:c.15369-263C>T	XP_011539416.1:n.15369-263C>T
XM_011541115.1:c.15363-263C>T	XP_011539417.1:n.15363-263C>T
XM_011541116.1:c.15354-263C>T	XP_011539418.1:n.15354-263C>T
XM_011541117.1:c.15303-263C>T	XP_011539419.1:n.15303-263C>T
XM_011541118.1:c.15300-263C>T	XP_011539420.1:n.15300-263C>T
XM_011541119.1:c.15267-263C>T	XP_011539421.1:n.15267-263C>T
XM_011541120.1:c.15264-263C>T	XP_011539422.1:n.15264-263C>T
XM_011541121.1:c.15231-263C>T	XP_011539423.1:n.15231-263C>T
XM_011541108.3:c.15501-263C>T	XP_011539410.2:n.15501-263C>T
XM_011541109.3:c.15498-263C>T	XP_011539411.2:n.15498-263C>T
XM_011541110.3:c.15498-263C>T	XP_011539412.2:n.15498-263C>T
XM_011541111.3:c.15498-263C>T	XP_011539413.2:n.15498-263C>T
XM_011541112.3:c.15486-263C>T	XP_011539414.2:n.15486-263C>T
XM_011541113.3:c.15483-263C>T	XP_011539415.2:n.15483-263C>T
XM_011541114.3:c.15483-263C>T	XP_011539416.2:n.15483-263C>T
XM_011541115.3:c.15477-263C>T	XP_011539417.2:n.15477-263C>T
XM_011541116.3:c.15468-263C>T	XP_011539418.2:n.15468-263C>T
XM_011541117.3:c.15417-263C>T	XP_011539419.2:n.15417-263C>T
XM_011541118.3:c.15414-263C>T	XP_011539420.2:n.15414-263C>T
XM_011541119.3:c.15381-263C>T	XP_011539421.2:n.15381-263C>T
XM_011541120.3:c.15378-263C>T	XP_011539422.2:n.15378-263C>T
XM_011541121.3:c.15345-263C>T	XP_011539423.2:n.15345-263C>T
XM_017000822.2:c.15480-263C>T	XP_016856311.2:n.15480-263C>T
XM_017000823.2:c.15453-263C>T	XP_016856312.2:n.15453-263C>T
XM_017000824.2:c.15399-263C>T	XP_016856313.2:n.15399-263C>T
XM_017000825.2:c.15384-263C>T	XP_016856314.2:n.15384-263C>T
XM_017000826.2:c.15381-263C>T	XP_016856315.2:n.15381-263C>T
XM_017000827.2:c.15366-263C>T	XP_016856316.2:n.15366-263C>T
XM_017000828.2:c.15342-263C>T	XP_016856317.2:n.15342-263C>T
XM_017000829.2:c.15294-263C>T	XP_016856318.2:n.15294-263C>T
XM_017000830.2:c.15243-263C>T	XP_016856319.2:n.15243-263C>T
NM_020765.3:c.15234-263C>T MANE Select	NP_065816.2:n.15234-263C>T