Canonical Allele Identifier: CA338748352

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404556T>C (hg19) ; chr1:g.19078062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078062T>C , CM000663.2:g.19078062T>C	GRCh38
NC_000001.10:g.19404556T>C , CM000663.1:g.19404556T>C	GRCh37
NC_000001.9:g.19277143T>C	NCBI36
NG_027669.1:g.137191A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15238A>G MANE Select	ENSP00000364403.3:p.Thr5080Ala
ENST00000375224.1:c.2359A>G	ENSP00000364372.1:p.Thr787Ala
ENST00000375225.7:c.463A>G	ENSP00000364373.3:p.Thr155Ala
ENST00000375254.7:c.15238A>G	ENSP00000364403.3:p.Thr5080Ala
ENST00000459947.5:n.3245A>G
NM_020765.2:c.15238A>G	NP_065816.2:p.Thr5080Ala
XM_011541108.1:c.15391A>G	XP_011539410.1:p.Thr5131Ala
XM_011541109.1:c.15388A>G	XP_011539411.1:p.Thr5130Ala
XM_011541110.1:c.15388A>G	XP_011539412.1:p.Thr5130Ala
XM_011541111.1:c.15388A>G	XP_011539413.1:p.Thr5130Ala
XM_011541112.1:c.15376A>G	XP_011539414.1:p.Thr5126Ala
XM_011541113.1:c.15373A>G	XP_011539415.1:p.Thr5125Ala
XM_011541114.1:c.15373A>G	XP_011539416.1:p.Thr5125Ala
XM_011541115.1:c.15367A>G	XP_011539417.1:p.Thr5123Ala
XM_011541116.1:c.15358A>G	XP_011539418.1:p.Thr5120Ala
XM_011541117.1:c.15307A>G	XP_011539419.1:p.Thr5103Ala
XM_011541118.1:c.15304A>G	XP_011539420.1:p.Thr5102Ala
XM_011541119.1:c.15271A>G	XP_011539421.1:p.Thr5091Ala
XM_011541120.1:c.15268A>G	XP_011539422.1:p.Thr5090Ala
XM_011541121.1:c.15235A>G	XP_011539423.1:p.Thr5079Ala
XM_011541108.3:c.15505A>G	XP_011539410.2:p.Thr5169Ala
XM_011541109.3:c.15502A>G	XP_011539411.2:p.Thr5168Ala
XM_011541110.3:c.15502A>G	XP_011539412.2:p.Thr5168Ala
XM_011541111.3:c.15502A>G	XP_011539413.2:p.Thr5168Ala
XM_011541112.3:c.15490A>G	XP_011539414.2:p.Thr5164Ala
XM_011541113.3:c.15487A>G	XP_011539415.2:p.Thr5163Ala
XM_011541114.3:c.15487A>G	XP_011539416.2:p.Thr5163Ala
XM_011541115.3:c.15481A>G	XP_011539417.2:p.Thr5161Ala
XM_011541116.3:c.15472A>G	XP_011539418.2:p.Thr5158Ala
XM_011541117.3:c.15421A>G	XP_011539419.2:p.Thr5141Ala
XM_011541118.3:c.15418A>G	XP_011539420.2:p.Thr5140Ala
XM_011541119.3:c.15385A>G	XP_011539421.2:p.Thr5129Ala
XM_011541120.3:c.15382A>G	XP_011539422.2:p.Thr5128Ala
XM_011541121.3:c.15349A>G	XP_011539423.2:p.Thr5117Ala
XM_017000822.2:c.15484A>G	XP_016856311.2:p.Thr5162Ala
XM_017000823.2:c.15457A>G	XP_016856312.2:p.Thr5153Ala
XM_017000824.2:c.15403A>G	XP_016856313.2:p.Thr5135Ala
XM_017000825.2:c.15388A>G	XP_016856314.2:p.Thr5130Ala
XM_017000826.2:c.15385A>G	XP_016856315.2:p.Thr5129Ala
XM_017000827.2:c.15370A>G	XP_016856316.2:p.Thr5124Ala
XM_017000828.2:c.15346A>G	XP_016856317.2:p.Thr5116Ala
XM_017000829.2:c.15298A>G	XP_016856318.2:p.Thr5100Ala
XM_017000830.2:c.15247A>G	XP_016856319.2:p.Thr5083Ala
NM_020765.3:c.15238A>G MANE Select	NP_065816.2:p.Thr5080Ala