Canonical Allele Identifier: CA338748361

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404560C>A (hg19) ; chr1:g.19078066C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078066C>A , CM000663.2:g.19078066C>A	GRCh38
NC_000001.10:g.19404560C>A , CM000663.1:g.19404560C>A	GRCh37
NC_000001.9:g.19277147C>A	NCBI36
NG_027669.1:g.137187G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15234G>T MANE Select	ENSP00000364403.3:p.Arg5078Ser
ENST00000375224.1:c.2355G>T	ENSP00000364372.1:p.Arg785Ser
ENST00000375225.7:c.459G>T	ENSP00000364373.3:p.Arg153Ser
ENST00000375254.7:c.15234G>T	ENSP00000364403.3:p.Arg5078Ser
ENST00000459947.5:n.3241G>T
NM_020765.2:c.15234G>T	NP_065816.2:p.Arg5078Ser
XM_011541108.1:c.15387G>T	XP_011539410.1:p.Arg5129Ser
XM_011541109.1:c.15384G>T	XP_011539411.1:p.Arg5128Ser
XM_011541110.1:c.15384G>T	XP_011539412.1:p.Arg5128Ser
XM_011541111.1:c.15384G>T	XP_011539413.1:p.Arg5128Ser
XM_011541112.1:c.15372G>T	XP_011539414.1:p.Arg5124Ser
XM_011541113.1:c.15369G>T	XP_011539415.1:p.Arg5123Ser
XM_011541114.1:c.15369G>T	XP_011539416.1:p.Arg5123Ser
XM_011541115.1:c.15363G>T	XP_011539417.1:p.Arg5121Ser
XM_011541116.1:c.15354G>T	XP_011539418.1:p.Arg5118Ser
XM_011541117.1:c.15303G>T	XP_011539419.1:p.Arg5101Ser
XM_011541118.1:c.15300G>T	XP_011539420.1:p.Arg5100Ser
XM_011541119.1:c.15267G>T	XP_011539421.1:p.Arg5089Ser
XM_011541120.1:c.15264G>T	XP_011539422.1:p.Arg5088Ser
XM_011541121.1:c.15231G>T	XP_011539423.1:p.Arg5077Ser
XM_011541108.3:c.15501G>T	XP_011539410.2:p.Arg5167Ser
XM_011541109.3:c.15498G>T	XP_011539411.2:p.Arg5166Ser
XM_011541110.3:c.15498G>T	XP_011539412.2:p.Arg5166Ser
XM_011541111.3:c.15498G>T	XP_011539413.2:p.Arg5166Ser
XM_011541112.3:c.15486G>T	XP_011539414.2:p.Arg5162Ser
XM_011541113.3:c.15483G>T	XP_011539415.2:p.Arg5161Ser
XM_011541114.3:c.15483G>T	XP_011539416.2:p.Arg5161Ser
XM_011541115.3:c.15477G>T	XP_011539417.2:p.Arg5159Ser
XM_011541116.3:c.15468G>T	XP_011539418.2:p.Arg5156Ser
XM_011541117.3:c.15417G>T	XP_011539419.2:p.Arg5139Ser
XM_011541118.3:c.15414G>T	XP_011539420.2:p.Arg5138Ser
XM_011541119.3:c.15381G>T	XP_011539421.2:p.Arg5127Ser
XM_011541120.3:c.15378G>T	XP_011539422.2:p.Arg5126Ser
XM_011541121.3:c.15345G>T	XP_011539423.2:p.Arg5115Ser
XM_017000822.2:c.15480G>T	XP_016856311.2:p.Arg5160Ser
XM_017000823.2:c.15453G>T	XP_016856312.2:p.Arg5151Ser
XM_017000824.2:c.15399G>T	XP_016856313.2:p.Arg5133Ser
XM_017000825.2:c.15384G>T	XP_016856314.2:p.Arg5128Ser
XM_017000826.2:c.15381G>T	XP_016856315.2:p.Arg5127Ser
XM_017000827.2:c.15366G>T	XP_016856316.2:p.Arg5122Ser
XM_017000828.2:c.15342G>T	XP_016856317.2:p.Arg5114Ser
XM_017000829.2:c.15294G>T	XP_016856318.2:p.Arg5098Ser
XM_017000830.2:c.15243G>T	XP_016856319.2:p.Arg5081Ser
NM_020765.3:c.15234G>T MANE Select	NP_065816.2:p.Arg5078Ser