Canonical Allele Identifier: CA338748131

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15302A>C MANE Select	ENSP00000364403.3:p.Asp5101Ala
ENST00000375224.1:c.2423A>C	ENSP00000364372.1:p.Asp808Ala
ENST00000375225.7:c.527A>C	ENSP00000364373.3:p.Asp176Ala
ENST00000375254.7:c.15302A>C	ENSP00000364403.3:p.Asp5101Ala
ENST00000459947.5:n.3309A>C
NM_020765.2:c.15302A>C	NP_065816.2:p.Asp5101Ala
XM_011541108.1:c.15455A>C	XP_011539410.1:p.Asp5152Ala
XM_011541109.1:c.15452A>C	XP_011539411.1:p.Asp5151Ala
XM_011541110.1:c.15452A>C	XP_011539412.1:p.Asp5151Ala
XM_011541111.1:c.15452A>C	XP_011539413.1:p.Asp5151Ala
XM_011541112.1:c.15440A>C	XP_011539414.1:p.Asp5147Ala
XM_011541113.1:c.15437A>C	XP_011539415.1:p.Asp5146Ala
XM_011541114.1:c.15437A>C	XP_011539416.1:p.Asp5146Ala
XM_011541115.1:c.15431A>C	XP_011539417.1:p.Asp5144Ala
XM_011541116.1:c.15422A>C	XP_011539418.1:p.Asp5141Ala
XM_011541117.1:c.15371A>C	XP_011539419.1:p.Asp5124Ala
XM_011541118.1:c.15368A>C	XP_011539420.1:p.Asp5123Ala
XM_011541119.1:c.15335A>C	XP_011539421.1:p.Asp5112Ala
XM_011541120.1:c.15332A>C	XP_011539422.1:p.Asp5111Ala
XM_011541121.1:c.15299A>C	XP_011539423.1:p.Asp5100Ala
XM_011541108.3:c.15569A>C	XP_011539410.2:p.Asp5190Ala
XM_011541109.3:c.15566A>C	XP_011539411.2:p.Asp5189Ala
XM_011541110.3:c.15566A>C	XP_011539412.2:p.Asp5189Ala
XM_011541111.3:c.15566A>C	XP_011539413.2:p.Asp5189Ala
XM_011541112.3:c.15554A>C	XP_011539414.2:p.Asp5185Ala
XM_011541113.3:c.15551A>C	XP_011539415.2:p.Asp5184Ala
XM_011541114.3:c.15551A>C	XP_011539416.2:p.Asp5184Ala
XM_011541115.3:c.15545A>C	XP_011539417.2:p.Asp5182Ala
XM_011541116.3:c.15536A>C	XP_011539418.2:p.Asp5179Ala
XM_011541117.3:c.15485A>C	XP_011539419.2:p.Asp5162Ala
XM_011541118.3:c.15482A>C	XP_011539420.2:p.Asp5161Ala
XM_011541119.3:c.15449A>C	XP_011539421.2:p.Asp5150Ala
XM_011541120.3:c.15446A>C	XP_011539422.2:p.Asp5149Ala
XM_011541121.3:c.15413A>C	XP_011539423.2:p.Asp5138Ala
XM_017000822.2:c.15548A>C	XP_016856311.2:p.Asp5183Ala
XM_017000823.2:c.15521A>C	XP_016856312.2:p.Asp5174Ala
XM_017000824.2:c.15467A>C	XP_016856313.2:p.Asp5156Ala
XM_017000825.2:c.15452A>C	XP_016856314.2:p.Asp5151Ala
XM_017000826.2:c.15449A>C	XP_016856315.2:p.Asp5150Ala
XM_017000827.2:c.15434A>C	XP_016856316.2:p.Asp5145Ala
XM_017000828.2:c.15410A>C	XP_016856317.2:p.Asp5137Ala
XM_017000829.2:c.15362A>C	XP_016856318.2:p.Asp5121Ala
XM_017000830.2:c.15311A>C	XP_016856319.2:p.Asp5104Ala
NM_020765.3:c.15302A>C MANE Select	NP_065816.2:p.Asp5101Ala