Canonical Allele Identifier: CA338748032

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404471T>C (hg19) ; chr1:g.19077977T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077977T>C , CM000663.2:g.19077977T>C	GRCh38
NC_000001.10:g.19404471T>C , CM000663.1:g.19404471T>C	GRCh37
NC_000001.9:g.19277058T>C	NCBI36
NG_027669.1:g.137276A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15323A>G MANE Select	ENSP00000364403.3:p.Lys5108Arg
ENST00000375224.1:c.2444A>G	ENSP00000364372.1:p.Lys815Arg
ENST00000375225.7:c.548A>G	ENSP00000364373.3:p.Lys183Arg
ENST00000375254.7:c.15323A>G	ENSP00000364403.3:p.Lys5108Arg
ENST00000459947.5:n.3330A>G
NM_020765.2:c.15323A>G	NP_065816.2:p.Lys5108Arg
XM_011541108.1:c.15476A>G	XP_011539410.1:p.Lys5159Arg
XM_011541109.1:c.15473A>G	XP_011539411.1:p.Lys5158Arg
XM_011541110.1:c.15473A>G	XP_011539412.1:p.Lys5158Arg
XM_011541111.1:c.15473A>G	XP_011539413.1:p.Lys5158Arg
XM_011541112.1:c.15461A>G	XP_011539414.1:p.Lys5154Arg
XM_011541113.1:c.15458A>G	XP_011539415.1:p.Lys5153Arg
XM_011541114.1:c.15458A>G	XP_011539416.1:p.Lys5153Arg
XM_011541115.1:c.15452A>G	XP_011539417.1:p.Lys5151Arg
XM_011541116.1:c.15443A>G	XP_011539418.1:p.Lys5148Arg
XM_011541117.1:c.15392A>G	XP_011539419.1:p.Lys5131Arg
XM_011541118.1:c.15389A>G	XP_011539420.1:p.Lys5130Arg
XM_011541119.1:c.15356A>G	XP_011539421.1:p.Lys5119Arg
XM_011541120.1:c.15353A>G	XP_011539422.1:p.Lys5118Arg
XM_011541121.1:c.15320A>G	XP_011539423.1:p.Lys5107Arg
XM_011541108.3:c.15590A>G	XP_011539410.2:p.Lys5197Arg
XM_011541109.3:c.15587A>G	XP_011539411.2:p.Lys5196Arg
XM_011541110.3:c.15587A>G	XP_011539412.2:p.Lys5196Arg
XM_011541111.3:c.15587A>G	XP_011539413.2:p.Lys5196Arg
XM_011541112.3:c.15575A>G	XP_011539414.2:p.Lys5192Arg
XM_011541113.3:c.15572A>G	XP_011539415.2:p.Lys5191Arg
XM_011541114.3:c.15572A>G	XP_011539416.2:p.Lys5191Arg
XM_011541115.3:c.15566A>G	XP_011539417.2:p.Lys5189Arg
XM_011541116.3:c.15557A>G	XP_011539418.2:p.Lys5186Arg
XM_011541117.3:c.15506A>G	XP_011539419.2:p.Lys5169Arg
XM_011541118.3:c.15503A>G	XP_011539420.2:p.Lys5168Arg
XM_011541119.3:c.15470A>G	XP_011539421.2:p.Lys5157Arg
XM_011541120.3:c.15467A>G	XP_011539422.2:p.Lys5156Arg
XM_011541121.3:c.15434A>G	XP_011539423.2:p.Lys5145Arg
XM_017000822.2:c.15569A>G	XP_016856311.2:p.Lys5190Arg
XM_017000823.2:c.15542A>G	XP_016856312.2:p.Lys5181Arg
XM_017000824.2:c.15488A>G	XP_016856313.2:p.Lys5163Arg
XM_017000825.2:c.15473A>G	XP_016856314.2:p.Lys5158Arg
XM_017000826.2:c.15470A>G	XP_016856315.2:p.Lys5157Arg
XM_017000827.2:c.15455A>G	XP_016856316.2:p.Lys5152Arg
XM_017000828.2:c.15431A>G	XP_016856317.2:p.Lys5144Arg
XM_017000829.2:c.15383A>G	XP_016856318.2:p.Lys5128Arg
XM_017000830.2:c.15332A>G	XP_016856319.2:p.Lys5111Arg
NM_020765.3:c.15323A>G MANE Select	NP_065816.2:p.Lys5108Arg