Canonical Allele Identifier: CA416453145

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404515G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078021G>C , CM000663.2:g.19078021G>C	GRCh38
NC_000001.10:g.19404515G>C , CM000663.1:g.19404515G>C	GRCh37
NC_000001.9:g.19277102G>C	NCBI36
NG_027669.1:g.137232C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15279C>G MANE Select	ENSP00000364403.3:p.Ser5093=
ENST00000375224.1:c.2400C>G	ENSP00000364372.1:p.Ser800=
ENST00000375225.7:c.504C>G	ENSP00000364373.3:p.Ser168=
ENST00000375254.7:c.15279C>G	ENSP00000364403.3:p.Ser5093=
ENST00000459947.5:n.3286C>G
NM_020765.2:c.15279C>G	NP_065816.2:p.Ser5093=
XM_011541108.1:c.15432C>G	XP_011539410.1:p.Ser5144=
XM_011541109.1:c.15429C>G	XP_011539411.1:p.Ser5143=
XM_011541110.1:c.15429C>G	XP_011539412.1:p.Ser5143=
XM_011541111.1:c.15429C>G	XP_011539413.1:p.Ser5143=
XM_011541112.1:c.15417C>G	XP_011539414.1:p.Ser5139=
XM_011541113.1:c.15414C>G	XP_011539415.1:p.Ser5138=
XM_011541114.1:c.15414C>G	XP_011539416.1:p.Ser5138=
XM_011541115.1:c.15408C>G	XP_011539417.1:p.Ser5136=
XM_011541116.1:c.15399C>G	XP_011539418.1:p.Ser5133=
XM_011541117.1:c.15348C>G	XP_011539419.1:p.Ser5116=
XM_011541118.1:c.15345C>G	XP_011539420.1:p.Ser5115=
XM_011541119.1:c.15312C>G	XP_011539421.1:p.Ser5104=
XM_011541120.1:c.15309C>G	XP_011539422.1:p.Ser5103=
XM_011541121.1:c.15276C>G	XP_011539423.1:p.Ser5092=
XM_011541108.3:c.15546C>G	XP_011539410.2:p.Ser5182=
XM_011541109.3:c.15543C>G	XP_011539411.2:p.Ser5181=
XM_011541110.3:c.15543C>G	XP_011539412.2:p.Ser5181=
XM_011541111.3:c.15543C>G	XP_011539413.2:p.Ser5181=
XM_011541112.3:c.15531C>G	XP_011539414.2:p.Ser5177=
XM_011541113.3:c.15528C>G	XP_011539415.2:p.Ser5176=
XM_011541114.3:c.15528C>G	XP_011539416.2:p.Ser5176=
XM_011541115.3:c.15522C>G	XP_011539417.2:p.Ser5174=
XM_011541116.3:c.15513C>G	XP_011539418.2:p.Ser5171=
XM_011541117.3:c.15462C>G	XP_011539419.2:p.Ser5154=
XM_011541118.3:c.15459C>G	XP_011539420.2:p.Ser5153=
XM_011541119.3:c.15426C>G	XP_011539421.2:p.Ser5142=
XM_011541120.3:c.15423C>G	XP_011539422.2:p.Ser5141=
XM_011541121.3:c.15390C>G	XP_011539423.2:p.Ser5130=
XM_017000822.2:c.15525C>G	XP_016856311.2:p.Ser5175=
XM_017000823.2:c.15498C>G	XP_016856312.2:p.Ser5166=
XM_017000824.2:c.15444C>G	XP_016856313.2:p.Ser5148=
XM_017000825.2:c.15429C>G	XP_016856314.2:p.Ser5143=
XM_017000826.2:c.15426C>G	XP_016856315.2:p.Ser5142=
XM_017000827.2:c.15411C>G	XP_016856316.2:p.Ser5137=
XM_017000828.2:c.15387C>G	XP_016856317.2:p.Ser5129=
XM_017000829.2:c.15339C>G	XP_016856318.2:p.Ser5113=
XM_017000830.2:c.15288C>G	XP_016856319.2:p.Ser5096=
NM_020765.3:c.15279C>G MANE Select	NP_065816.2:p.Ser5093=