Canonical Allele Identifier: CA416453154

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404524G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078030G>A , CM000663.2:g.19078030G>A	GRCh38
NC_000001.10:g.19404524G>A , CM000663.1:g.19404524G>A	GRCh37
NC_000001.9:g.19277111G>A	NCBI36
NG_027669.1:g.137223C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15270C>T MANE Select	ENSP00000364403.3:p.Tyr5090=
ENST00000375224.1:c.2391C>T	ENSP00000364372.1:p.Tyr797=
ENST00000375225.7:c.495C>T	ENSP00000364373.3:p.Tyr165=
ENST00000375254.7:c.15270C>T	ENSP00000364403.3:p.Tyr5090=
ENST00000459947.5:n.3277C>T
NM_020765.2:c.15270C>T	NP_065816.2:p.Tyr5090=
XM_011541108.1:c.15423C>T	XP_011539410.1:p.Tyr5141=
XM_011541109.1:c.15420C>T	XP_011539411.1:p.Tyr5140=
XM_011541110.1:c.15420C>T	XP_011539412.1:p.Tyr5140=
XM_011541111.1:c.15420C>T	XP_011539413.1:p.Tyr5140=
XM_011541112.1:c.15408C>T	XP_011539414.1:p.Tyr5136=
XM_011541113.1:c.15405C>T	XP_011539415.1:p.Tyr5135=
XM_011541114.1:c.15405C>T	XP_011539416.1:p.Tyr5135=
XM_011541115.1:c.15399C>T	XP_011539417.1:p.Tyr5133=
XM_011541116.1:c.15390C>T	XP_011539418.1:p.Tyr5130=
XM_011541117.1:c.15339C>T	XP_011539419.1:p.Tyr5113=
XM_011541118.1:c.15336C>T	XP_011539420.1:p.Tyr5112=
XM_011541119.1:c.15303C>T	XP_011539421.1:p.Tyr5101=
XM_011541120.1:c.15300C>T	XP_011539422.1:p.Tyr5100=
XM_011541121.1:c.15267C>T	XP_011539423.1:p.Tyr5089=
XM_011541108.3:c.15537C>T	XP_011539410.2:p.Tyr5179=
XM_011541109.3:c.15534C>T	XP_011539411.2:p.Tyr5178=
XM_011541110.3:c.15534C>T	XP_011539412.2:p.Tyr5178=
XM_011541111.3:c.15534C>T	XP_011539413.2:p.Tyr5178=
XM_011541112.3:c.15522C>T	XP_011539414.2:p.Tyr5174=
XM_011541113.3:c.15519C>T	XP_011539415.2:p.Tyr5173=
XM_011541114.3:c.15519C>T	XP_011539416.2:p.Tyr5173=
XM_011541115.3:c.15513C>T	XP_011539417.2:p.Tyr5171=
XM_011541116.3:c.15504C>T	XP_011539418.2:p.Tyr5168=
XM_011541117.3:c.15453C>T	XP_011539419.2:p.Tyr5151=
XM_011541118.3:c.15450C>T	XP_011539420.2:p.Tyr5150=
XM_011541119.3:c.15417C>T	XP_011539421.2:p.Tyr5139=
XM_011541120.3:c.15414C>T	XP_011539422.2:p.Tyr5138=
XM_011541121.3:c.15381C>T	XP_011539423.2:p.Tyr5127=
XM_017000822.2:c.15516C>T	XP_016856311.2:p.Tyr5172=
XM_017000823.2:c.15489C>T	XP_016856312.2:p.Tyr5163=
XM_017000824.2:c.15435C>T	XP_016856313.2:p.Tyr5145=
XM_017000825.2:c.15420C>T	XP_016856314.2:p.Tyr5140=
XM_017000826.2:c.15417C>T	XP_016856315.2:p.Tyr5139=
XM_017000827.2:c.15402C>T	XP_016856316.2:p.Tyr5134=
XM_017000828.2:c.15378C>T	XP_016856317.2:p.Tyr5126=
XM_017000829.2:c.15330C>T	XP_016856318.2:p.Tyr5110=
XM_017000830.2:c.15279C>T	XP_016856319.2:p.Tyr5093=
NM_020765.3:c.15270C>T MANE Select	NP_065816.2:p.Tyr5090=