Canonical Allele Identifier: CA338748196

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404517A>G (hg19) ; chr1:g.19078023A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078023A>G , CM000663.2:g.19078023A>G	GRCh38
NC_000001.10:g.19404517A>G , CM000663.1:g.19404517A>G	GRCh37
NC_000001.9:g.19277104A>G	NCBI36
NG_027669.1:g.137230T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15277T>C MANE Select	ENSP00000364403.3:p.Ser5093Pro
ENST00000375224.1:c.2398T>C	ENSP00000364372.1:p.Ser800Pro
ENST00000375225.7:c.502T>C	ENSP00000364373.3:p.Ser168Pro
ENST00000375254.7:c.15277T>C	ENSP00000364403.3:p.Ser5093Pro
ENST00000459947.5:n.3284T>C
NM_020765.2:c.15277T>C	NP_065816.2:p.Ser5093Pro
XM_011541108.1:c.15430T>C	XP_011539410.1:p.Ser5144Pro
XM_011541109.1:c.15427T>C	XP_011539411.1:p.Ser5143Pro
XM_011541110.1:c.15427T>C	XP_011539412.1:p.Ser5143Pro
XM_011541111.1:c.15427T>C	XP_011539413.1:p.Ser5143Pro
XM_011541112.1:c.15415T>C	XP_011539414.1:p.Ser5139Pro
XM_011541113.1:c.15412T>C	XP_011539415.1:p.Ser5138Pro
XM_011541114.1:c.15412T>C	XP_011539416.1:p.Ser5138Pro
XM_011541115.1:c.15406T>C	XP_011539417.1:p.Ser5136Pro
XM_011541116.1:c.15397T>C	XP_011539418.1:p.Ser5133Pro
XM_011541117.1:c.15346T>C	XP_011539419.1:p.Ser5116Pro
XM_011541118.1:c.15343T>C	XP_011539420.1:p.Ser5115Pro
XM_011541119.1:c.15310T>C	XP_011539421.1:p.Ser5104Pro
XM_011541120.1:c.15307T>C	XP_011539422.1:p.Ser5103Pro
XM_011541121.1:c.15274T>C	XP_011539423.1:p.Ser5092Pro
XM_011541108.3:c.15544T>C	XP_011539410.2:p.Ser5182Pro
XM_011541109.3:c.15541T>C	XP_011539411.2:p.Ser5181Pro
XM_011541110.3:c.15541T>C	XP_011539412.2:p.Ser5181Pro
XM_011541111.3:c.15541T>C	XP_011539413.2:p.Ser5181Pro
XM_011541112.3:c.15529T>C	XP_011539414.2:p.Ser5177Pro
XM_011541113.3:c.15526T>C	XP_011539415.2:p.Ser5176Pro
XM_011541114.3:c.15526T>C	XP_011539416.2:p.Ser5176Pro
XM_011541115.3:c.15520T>C	XP_011539417.2:p.Ser5174Pro
XM_011541116.3:c.15511T>C	XP_011539418.2:p.Ser5171Pro
XM_011541117.3:c.15460T>C	XP_011539419.2:p.Ser5154Pro
XM_011541118.3:c.15457T>C	XP_011539420.2:p.Ser5153Pro
XM_011541119.3:c.15424T>C	XP_011539421.2:p.Ser5142Pro
XM_011541120.3:c.15421T>C	XP_011539422.2:p.Ser5141Pro
XM_011541121.3:c.15388T>C	XP_011539423.2:p.Ser5130Pro
XM_017000822.2:c.15523T>C	XP_016856311.2:p.Ser5175Pro
XM_017000823.2:c.15496T>C	XP_016856312.2:p.Ser5166Pro
XM_017000824.2:c.15442T>C	XP_016856313.2:p.Ser5148Pro
XM_017000825.2:c.15427T>C	XP_016856314.2:p.Ser5143Pro
XM_017000826.2:c.15424T>C	XP_016856315.2:p.Ser5142Pro
XM_017000827.2:c.15409T>C	XP_016856316.2:p.Ser5137Pro
XM_017000828.2:c.15385T>C	XP_016856317.2:p.Ser5129Pro
XM_017000829.2:c.15337T>C	XP_016856318.2:p.Ser5113Pro
XM_017000830.2:c.15286T>C	XP_016856319.2:p.Ser5096Pro
NM_020765.3:c.15277T>C MANE Select	NP_065816.2:p.Ser5093Pro