Canonical Allele Identifier: CA338748129

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404492T>A (hg19) ; chr1:g.19077998T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077998T>A , CM000663.2:g.19077998T>A	GRCh38
NC_000001.10:g.19404492T>A , CM000663.1:g.19404492T>A	GRCh37
NC_000001.9:g.19277079T>A	NCBI36
NG_027669.1:g.137255A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15302A>T MANE Select	ENSP00000364403.3:p.Asp5101Val
ENST00000375224.1:c.2423A>T	ENSP00000364372.1:p.Asp808Val
ENST00000375225.7:c.527A>T	ENSP00000364373.3:p.Asp176Val
ENST00000375254.7:c.15302A>T	ENSP00000364403.3:p.Asp5101Val
ENST00000459947.5:n.3309A>T
NM_020765.2:c.15302A>T	NP_065816.2:p.Asp5101Val
XM_011541108.1:c.15455A>T	XP_011539410.1:p.Asp5152Val
XM_011541109.1:c.15452A>T	XP_011539411.1:p.Asp5151Val
XM_011541110.1:c.15452A>T	XP_011539412.1:p.Asp5151Val
XM_011541111.1:c.15452A>T	XP_011539413.1:p.Asp5151Val
XM_011541112.1:c.15440A>T	XP_011539414.1:p.Asp5147Val
XM_011541113.1:c.15437A>T	XP_011539415.1:p.Asp5146Val
XM_011541114.1:c.15437A>T	XP_011539416.1:p.Asp5146Val
XM_011541115.1:c.15431A>T	XP_011539417.1:p.Asp5144Val
XM_011541116.1:c.15422A>T	XP_011539418.1:p.Asp5141Val
XM_011541117.1:c.15371A>T	XP_011539419.1:p.Asp5124Val
XM_011541118.1:c.15368A>T	XP_011539420.1:p.Asp5123Val
XM_011541119.1:c.15335A>T	XP_011539421.1:p.Asp5112Val
XM_011541120.1:c.15332A>T	XP_011539422.1:p.Asp5111Val
XM_011541121.1:c.15299A>T	XP_011539423.1:p.Asp5100Val
XM_011541108.3:c.15569A>T	XP_011539410.2:p.Asp5190Val
XM_011541109.3:c.15566A>T	XP_011539411.2:p.Asp5189Val
XM_011541110.3:c.15566A>T	XP_011539412.2:p.Asp5189Val
XM_011541111.3:c.15566A>T	XP_011539413.2:p.Asp5189Val
XM_011541112.3:c.15554A>T	XP_011539414.2:p.Asp5185Val
XM_011541113.3:c.15551A>T	XP_011539415.2:p.Asp5184Val
XM_011541114.3:c.15551A>T	XP_011539416.2:p.Asp5184Val
XM_011541115.3:c.15545A>T	XP_011539417.2:p.Asp5182Val
XM_011541116.3:c.15536A>T	XP_011539418.2:p.Asp5179Val
XM_011541117.3:c.15485A>T	XP_011539419.2:p.Asp5162Val
XM_011541118.3:c.15482A>T	XP_011539420.2:p.Asp5161Val
XM_011541119.3:c.15449A>T	XP_011539421.2:p.Asp5150Val
XM_011541120.3:c.15446A>T	XP_011539422.2:p.Asp5149Val
XM_011541121.3:c.15413A>T	XP_011539423.2:p.Asp5138Val
XM_017000822.2:c.15548A>T	XP_016856311.2:p.Asp5183Val
XM_017000823.2:c.15521A>T	XP_016856312.2:p.Asp5174Val
XM_017000824.2:c.15467A>T	XP_016856313.2:p.Asp5156Val
XM_017000825.2:c.15452A>T	XP_016856314.2:p.Asp5151Val
XM_017000826.2:c.15449A>T	XP_016856315.2:p.Asp5150Val
XM_017000827.2:c.15434A>T	XP_016856316.2:p.Asp5145Val
XM_017000828.2:c.15410A>T	XP_016856317.2:p.Asp5137Val
XM_017000829.2:c.15362A>T	XP_016856318.2:p.Asp5121Val
XM_017000830.2:c.15311A>T	XP_016856319.2:p.Asp5104Val
NM_020765.3:c.15302A>T MANE Select	NP_065816.2:p.Asp5101Val