Canonical Allele Identifier: CA338748133

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404493C>A (hg19) ; chr1:g.19077999C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077999C>A , CM000663.2:g.19077999C>A	GRCh38
NC_000001.10:g.19404493C>A , CM000663.1:g.19404493C>A	GRCh37
NC_000001.9:g.19277080C>A	NCBI36
NG_027669.1:g.137254G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15301G>T MANE Select	ENSP00000364403.3:p.Asp5101Tyr
ENST00000375224.1:c.2422G>T	ENSP00000364372.1:p.Asp808Tyr
ENST00000375225.7:c.526G>T	ENSP00000364373.3:p.Asp176Tyr
ENST00000375254.7:c.15301G>T	ENSP00000364403.3:p.Asp5101Tyr
ENST00000459947.5:n.3308G>T
NM_020765.2:c.15301G>T	NP_065816.2:p.Asp5101Tyr
XM_011541108.1:c.15454G>T	XP_011539410.1:p.Asp5152Tyr
XM_011541109.1:c.15451G>T	XP_011539411.1:p.Asp5151Tyr
XM_011541110.1:c.15451G>T	XP_011539412.1:p.Asp5151Tyr
XM_011541111.1:c.15451G>T	XP_011539413.1:p.Asp5151Tyr
XM_011541112.1:c.15439G>T	XP_011539414.1:p.Asp5147Tyr
XM_011541113.1:c.15436G>T	XP_011539415.1:p.Asp5146Tyr
XM_011541114.1:c.15436G>T	XP_011539416.1:p.Asp5146Tyr
XM_011541115.1:c.15430G>T	XP_011539417.1:p.Asp5144Tyr
XM_011541116.1:c.15421G>T	XP_011539418.1:p.Asp5141Tyr
XM_011541117.1:c.15370G>T	XP_011539419.1:p.Asp5124Tyr
XM_011541118.1:c.15367G>T	XP_011539420.1:p.Asp5123Tyr
XM_011541119.1:c.15334G>T	XP_011539421.1:p.Asp5112Tyr
XM_011541120.1:c.15331G>T	XP_011539422.1:p.Asp5111Tyr
XM_011541121.1:c.15298G>T	XP_011539423.1:p.Asp5100Tyr
XM_011541108.3:c.15568G>T	XP_011539410.2:p.Asp5190Tyr
XM_011541109.3:c.15565G>T	XP_011539411.2:p.Asp5189Tyr
XM_011541110.3:c.15565G>T	XP_011539412.2:p.Asp5189Tyr
XM_011541111.3:c.15565G>T	XP_011539413.2:p.Asp5189Tyr
XM_011541112.3:c.15553G>T	XP_011539414.2:p.Asp5185Tyr
XM_011541113.3:c.15550G>T	XP_011539415.2:p.Asp5184Tyr
XM_011541114.3:c.15550G>T	XP_011539416.2:p.Asp5184Tyr
XM_011541115.3:c.15544G>T	XP_011539417.2:p.Asp5182Tyr
XM_011541116.3:c.15535G>T	XP_011539418.2:p.Asp5179Tyr
XM_011541117.3:c.15484G>T	XP_011539419.2:p.Asp5162Tyr
XM_011541118.3:c.15481G>T	XP_011539420.2:p.Asp5161Tyr
XM_011541119.3:c.15448G>T	XP_011539421.2:p.Asp5150Tyr
XM_011541120.3:c.15445G>T	XP_011539422.2:p.Asp5149Tyr
XM_011541121.3:c.15412G>T	XP_011539423.2:p.Asp5138Tyr
XM_017000822.2:c.15547G>T	XP_016856311.2:p.Asp5183Tyr
XM_017000823.2:c.15520G>T	XP_016856312.2:p.Asp5174Tyr
XM_017000824.2:c.15466G>T	XP_016856313.2:p.Asp5156Tyr
XM_017000825.2:c.15451G>T	XP_016856314.2:p.Asp5151Tyr
XM_017000826.2:c.15448G>T	XP_016856315.2:p.Asp5150Tyr
XM_017000827.2:c.15433G>T	XP_016856316.2:p.Asp5145Tyr
XM_017000828.2:c.15409G>T	XP_016856317.2:p.Asp5137Tyr
XM_017000829.2:c.15361G>T	XP_016856318.2:p.Asp5121Tyr
XM_017000830.2:c.15310G>T	XP_016856319.2:p.Asp5104Tyr
NM_020765.3:c.15301G>T MANE Select	NP_065816.2:p.Asp5101Tyr