Canonical Allele Identifier: CA338748113

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404489A>C (hg19) ; chr1:g.19077995A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077995A>C , CM000663.2:g.19077995A>C	GRCh38
NC_000001.10:g.19404489A>C , CM000663.1:g.19404489A>C	GRCh37
NC_000001.9:g.19277076A>C	NCBI36
NG_027669.1:g.137258T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15305T>G MANE Select	ENSP00000364403.3:p.Leu5102Arg
ENST00000375224.1:c.2426T>G	ENSP00000364372.1:p.Leu809Arg
ENST00000375225.7:c.530T>G	ENSP00000364373.3:p.Leu177Arg
ENST00000375254.7:c.15305T>G	ENSP00000364403.3:p.Leu5102Arg
ENST00000459947.5:n.3312T>G
NM_020765.2:c.15305T>G	NP_065816.2:p.Leu5102Arg
XM_011541108.1:c.15458T>G	XP_011539410.1:p.Leu5153Arg
XM_011541109.1:c.15455T>G	XP_011539411.1:p.Leu5152Arg
XM_011541110.1:c.15455T>G	XP_011539412.1:p.Leu5152Arg
XM_011541111.1:c.15455T>G	XP_011539413.1:p.Leu5152Arg
XM_011541112.1:c.15443T>G	XP_011539414.1:p.Leu5148Arg
XM_011541113.1:c.15440T>G	XP_011539415.1:p.Leu5147Arg
XM_011541114.1:c.15440T>G	XP_011539416.1:p.Leu5147Arg
XM_011541115.1:c.15434T>G	XP_011539417.1:p.Leu5145Arg
XM_011541116.1:c.15425T>G	XP_011539418.1:p.Leu5142Arg
XM_011541117.1:c.15374T>G	XP_011539419.1:p.Leu5125Arg
XM_011541118.1:c.15371T>G	XP_011539420.1:p.Leu5124Arg
XM_011541119.1:c.15338T>G	XP_011539421.1:p.Leu5113Arg
XM_011541120.1:c.15335T>G	XP_011539422.1:p.Leu5112Arg
XM_011541121.1:c.15302T>G	XP_011539423.1:p.Leu5101Arg
XM_011541108.3:c.15572T>G	XP_011539410.2:p.Leu5191Arg
XM_011541109.3:c.15569T>G	XP_011539411.2:p.Leu5190Arg
XM_011541110.3:c.15569T>G	XP_011539412.2:p.Leu5190Arg
XM_011541111.3:c.15569T>G	XP_011539413.2:p.Leu5190Arg
XM_011541112.3:c.15557T>G	XP_011539414.2:p.Leu5186Arg
XM_011541113.3:c.15554T>G	XP_011539415.2:p.Leu5185Arg
XM_011541114.3:c.15554T>G	XP_011539416.2:p.Leu5185Arg
XM_011541115.3:c.15548T>G	XP_011539417.2:p.Leu5183Arg
XM_011541116.3:c.15539T>G	XP_011539418.2:p.Leu5180Arg
XM_011541117.3:c.15488T>G	XP_011539419.2:p.Leu5163Arg
XM_011541118.3:c.15485T>G	XP_011539420.2:p.Leu5162Arg
XM_011541119.3:c.15452T>G	XP_011539421.2:p.Leu5151Arg
XM_011541120.3:c.15449T>G	XP_011539422.2:p.Leu5150Arg
XM_011541121.3:c.15416T>G	XP_011539423.2:p.Leu5139Arg
XM_017000822.2:c.15551T>G	XP_016856311.2:p.Leu5184Arg
XM_017000823.2:c.15524T>G	XP_016856312.2:p.Leu5175Arg
XM_017000824.2:c.15470T>G	XP_016856313.2:p.Leu5157Arg
XM_017000825.2:c.15455T>G	XP_016856314.2:p.Leu5152Arg
XM_017000826.2:c.15452T>G	XP_016856315.2:p.Leu5151Arg
XM_017000827.2:c.15437T>G	XP_016856316.2:p.Leu5146Arg
XM_017000828.2:c.15413T>G	XP_016856317.2:p.Leu5138Arg
XM_017000829.2:c.15365T>G	XP_016856318.2:p.Leu5122Arg
XM_017000830.2:c.15314T>G	XP_016856319.2:p.Leu5105Arg
NM_020765.3:c.15305T>G MANE Select	NP_065816.2:p.Leu5102Arg