Canonical Allele Identifier: CA416453122

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404509G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078015G>C , CM000663.2:g.19078015G>C	GRCh38
NC_000001.10:g.19404509G>C , CM000663.1:g.19404509G>C	GRCh37
NC_000001.9:g.19277096G>C	NCBI36
NG_027669.1:g.137238C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15285C>G MANE Select	ENSP00000364403.3:p.Leu5095=
ENST00000375224.1:c.2406C>G	ENSP00000364372.1:p.Leu802=
ENST00000375225.7:c.510C>G	ENSP00000364373.3:p.Leu170=
ENST00000375254.7:c.15285C>G	ENSP00000364403.3:p.Leu5095=
ENST00000459947.5:n.3292C>G
NM_020765.2:c.15285C>G	NP_065816.2:p.Leu5095=
XM_011541108.1:c.15438C>G	XP_011539410.1:p.Leu5146=
XM_011541109.1:c.15435C>G	XP_011539411.1:p.Leu5145=
XM_011541110.1:c.15435C>G	XP_011539412.1:p.Leu5145=
XM_011541111.1:c.15435C>G	XP_011539413.1:p.Leu5145=
XM_011541112.1:c.15423C>G	XP_011539414.1:p.Leu5141=
XM_011541113.1:c.15420C>G	XP_011539415.1:p.Leu5140=
XM_011541114.1:c.15420C>G	XP_011539416.1:p.Leu5140=
XM_011541115.1:c.15414C>G	XP_011539417.1:p.Leu5138=
XM_011541116.1:c.15405C>G	XP_011539418.1:p.Leu5135=
XM_011541117.1:c.15354C>G	XP_011539419.1:p.Leu5118=
XM_011541118.1:c.15351C>G	XP_011539420.1:p.Leu5117=
XM_011541119.1:c.15318C>G	XP_011539421.1:p.Leu5106=
XM_011541120.1:c.15315C>G	XP_011539422.1:p.Leu5105=
XM_011541121.1:c.15282C>G	XP_011539423.1:p.Leu5094=
XM_011541108.3:c.15552C>G	XP_011539410.2:p.Leu5184=
XM_011541109.3:c.15549C>G	XP_011539411.2:p.Leu5183=
XM_011541110.3:c.15549C>G	XP_011539412.2:p.Leu5183=
XM_011541111.3:c.15549C>G	XP_011539413.2:p.Leu5183=
XM_011541112.3:c.15537C>G	XP_011539414.2:p.Leu5179=
XM_011541113.3:c.15534C>G	XP_011539415.2:p.Leu5178=
XM_011541114.3:c.15534C>G	XP_011539416.2:p.Leu5178=
XM_011541115.3:c.15528C>G	XP_011539417.2:p.Leu5176=
XM_011541116.3:c.15519C>G	XP_011539418.2:p.Leu5173=
XM_011541117.3:c.15468C>G	XP_011539419.2:p.Leu5156=
XM_011541118.3:c.15465C>G	XP_011539420.2:p.Leu5155=
XM_011541119.3:c.15432C>G	XP_011539421.2:p.Leu5144=
XM_011541120.3:c.15429C>G	XP_011539422.2:p.Leu5143=
XM_011541121.3:c.15396C>G	XP_011539423.2:p.Leu5132=
XM_017000822.2:c.15531C>G	XP_016856311.2:p.Leu5177=
XM_017000823.2:c.15504C>G	XP_016856312.2:p.Leu5168=
XM_017000824.2:c.15450C>G	XP_016856313.2:p.Leu5150=
XM_017000825.2:c.15435C>G	XP_016856314.2:p.Leu5145=
XM_017000826.2:c.15432C>G	XP_016856315.2:p.Leu5144=
XM_017000827.2:c.15417C>G	XP_016856316.2:p.Leu5139=
XM_017000828.2:c.15393C>G	XP_016856317.2:p.Leu5131=
XM_017000829.2:c.15345C>G	XP_016856318.2:p.Leu5115=
XM_017000830.2:c.15294C>G	XP_016856319.2:p.Leu5098=
NM_020765.3:c.15285C>G MANE Select	NP_065816.2:p.Leu5095=