Canonical Allele Identifier: CA338748130

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15302A>G MANE Select	ENSP00000364403.3:p.Asp5101Gly
ENST00000375224.1:c.2423A>G	ENSP00000364372.1:p.Asp808Gly
ENST00000375225.7:c.527A>G	ENSP00000364373.3:p.Asp176Gly
ENST00000375254.7:c.15302A>G	ENSP00000364403.3:p.Asp5101Gly
ENST00000459947.5:n.3309A>G
NM_020765.2:c.15302A>G	NP_065816.2:p.Asp5101Gly
XM_011541108.1:c.15455A>G	XP_011539410.1:p.Asp5152Gly
XM_011541109.1:c.15452A>G	XP_011539411.1:p.Asp5151Gly
XM_011541110.1:c.15452A>G	XP_011539412.1:p.Asp5151Gly
XM_011541111.1:c.15452A>G	XP_011539413.1:p.Asp5151Gly
XM_011541112.1:c.15440A>G	XP_011539414.1:p.Asp5147Gly
XM_011541113.1:c.15437A>G	XP_011539415.1:p.Asp5146Gly
XM_011541114.1:c.15437A>G	XP_011539416.1:p.Asp5146Gly
XM_011541115.1:c.15431A>G	XP_011539417.1:p.Asp5144Gly
XM_011541116.1:c.15422A>G	XP_011539418.1:p.Asp5141Gly
XM_011541117.1:c.15371A>G	XP_011539419.1:p.Asp5124Gly
XM_011541118.1:c.15368A>G	XP_011539420.1:p.Asp5123Gly
XM_011541119.1:c.15335A>G	XP_011539421.1:p.Asp5112Gly
XM_011541120.1:c.15332A>G	XP_011539422.1:p.Asp5111Gly
XM_011541121.1:c.15299A>G	XP_011539423.1:p.Asp5100Gly
XM_011541108.3:c.15569A>G	XP_011539410.2:p.Asp5190Gly
XM_011541109.3:c.15566A>G	XP_011539411.2:p.Asp5189Gly
XM_011541110.3:c.15566A>G	XP_011539412.2:p.Asp5189Gly
XM_011541111.3:c.15566A>G	XP_011539413.2:p.Asp5189Gly
XM_011541112.3:c.15554A>G	XP_011539414.2:p.Asp5185Gly
XM_011541113.3:c.15551A>G	XP_011539415.2:p.Asp5184Gly
XM_011541114.3:c.15551A>G	XP_011539416.2:p.Asp5184Gly
XM_011541115.3:c.15545A>G	XP_011539417.2:p.Asp5182Gly
XM_011541116.3:c.15536A>G	XP_011539418.2:p.Asp5179Gly
XM_011541117.3:c.15485A>G	XP_011539419.2:p.Asp5162Gly
XM_011541118.3:c.15482A>G	XP_011539420.2:p.Asp5161Gly
XM_011541119.3:c.15449A>G	XP_011539421.2:p.Asp5150Gly
XM_011541120.3:c.15446A>G	XP_011539422.2:p.Asp5149Gly
XM_011541121.3:c.15413A>G	XP_011539423.2:p.Asp5138Gly
XM_017000822.2:c.15548A>G	XP_016856311.2:p.Asp5183Gly
XM_017000823.2:c.15521A>G	XP_016856312.2:p.Asp5174Gly
XM_017000824.2:c.15467A>G	XP_016856313.2:p.Asp5156Gly
XM_017000825.2:c.15452A>G	XP_016856314.2:p.Asp5151Gly
XM_017000826.2:c.15449A>G	XP_016856315.2:p.Asp5150Gly
XM_017000827.2:c.15434A>G	XP_016856316.2:p.Asp5145Gly
XM_017000828.2:c.15410A>G	XP_016856317.2:p.Asp5137Gly
XM_017000829.2:c.15362A>G	XP_016856318.2:p.Asp5121Gly
XM_017000830.2:c.15311A>G	XP_016856319.2:p.Asp5104Gly
NM_020765.3:c.15302A>G MANE Select	NP_065816.2:p.Asp5101Gly