Canonical Allele Identifier: CA338748066

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404477A>T (hg19) ; chr1:g.19077983A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077983A>T , CM000663.2:g.19077983A>T	GRCh38
NC_000001.10:g.19404477A>T , CM000663.1:g.19404477A>T	GRCh37
NC_000001.9:g.19277064A>T	NCBI36
NG_027669.1:g.137270T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15317T>A MANE Select	ENSP00000364403.3:p.Met5106Lys
ENST00000375224.1:c.2438T>A	ENSP00000364372.1:p.Met813Lys
ENST00000375225.7:c.542T>A	ENSP00000364373.3:p.Met181Lys
ENST00000375254.7:c.15317T>A	ENSP00000364403.3:p.Met5106Lys
ENST00000459947.5:n.3324T>A
NM_020765.2:c.15317T>A	NP_065816.2:p.Met5106Lys
XM_011541108.1:c.15470T>A	XP_011539410.1:p.Met5157Lys
XM_011541109.1:c.15467T>A	XP_011539411.1:p.Met5156Lys
XM_011541110.1:c.15467T>A	XP_011539412.1:p.Met5156Lys
XM_011541111.1:c.15467T>A	XP_011539413.1:p.Met5156Lys
XM_011541112.1:c.15455T>A	XP_011539414.1:p.Met5152Lys
XM_011541113.1:c.15452T>A	XP_011539415.1:p.Met5151Lys
XM_011541114.1:c.15452T>A	XP_011539416.1:p.Met5151Lys
XM_011541115.1:c.15446T>A	XP_011539417.1:p.Met5149Lys
XM_011541116.1:c.15437T>A	XP_011539418.1:p.Met5146Lys
XM_011541117.1:c.15386T>A	XP_011539419.1:p.Met5129Lys
XM_011541118.1:c.15383T>A	XP_011539420.1:p.Met5128Lys
XM_011541119.1:c.15350T>A	XP_011539421.1:p.Met5117Lys
XM_011541120.1:c.15347T>A	XP_011539422.1:p.Met5116Lys
XM_011541121.1:c.15314T>A	XP_011539423.1:p.Met5105Lys
XM_011541108.3:c.15584T>A	XP_011539410.2:p.Met5195Lys
XM_011541109.3:c.15581T>A	XP_011539411.2:p.Met5194Lys
XM_011541110.3:c.15581T>A	XP_011539412.2:p.Met5194Lys
XM_011541111.3:c.15581T>A	XP_011539413.2:p.Met5194Lys
XM_011541112.3:c.15569T>A	XP_011539414.2:p.Met5190Lys
XM_011541113.3:c.15566T>A	XP_011539415.2:p.Met5189Lys
XM_011541114.3:c.15566T>A	XP_011539416.2:p.Met5189Lys
XM_011541115.3:c.15560T>A	XP_011539417.2:p.Met5187Lys
XM_011541116.3:c.15551T>A	XP_011539418.2:p.Met5184Lys
XM_011541117.3:c.15500T>A	XP_011539419.2:p.Met5167Lys
XM_011541118.3:c.15497T>A	XP_011539420.2:p.Met5166Lys
XM_011541119.3:c.15464T>A	XP_011539421.2:p.Met5155Lys
XM_011541120.3:c.15461T>A	XP_011539422.2:p.Met5154Lys
XM_011541121.3:c.15428T>A	XP_011539423.2:p.Met5143Lys
XM_017000822.2:c.15563T>A	XP_016856311.2:p.Met5188Lys
XM_017000823.2:c.15536T>A	XP_016856312.2:p.Met5179Lys
XM_017000824.2:c.15482T>A	XP_016856313.2:p.Met5161Lys
XM_017000825.2:c.15467T>A	XP_016856314.2:p.Met5156Lys
XM_017000826.2:c.15464T>A	XP_016856315.2:p.Met5155Lys
XM_017000827.2:c.15449T>A	XP_016856316.2:p.Met5150Lys
XM_017000828.2:c.15425T>A	XP_016856317.2:p.Met5142Lys
XM_017000829.2:c.15377T>A	XP_016856318.2:p.Met5126Lys
XM_017000830.2:c.15326T>A	XP_016856319.2:p.Met5109Lys
NM_020765.3:c.15317T>A MANE Select	NP_065816.2:p.Met5106Lys