Canonical Allele Identifier: CA338748030

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15323A>T MANE Select	ENSP00000364403.3:p.Lys5108Met
ENST00000375224.1:c.2444A>T	ENSP00000364372.1:p.Lys815Met
ENST00000375225.7:c.548A>T	ENSP00000364373.3:p.Lys183Met
ENST00000375254.7:c.15323A>T	ENSP00000364403.3:p.Lys5108Met
ENST00000459947.5:n.3330A>T
NM_020765.2:c.15323A>T	NP_065816.2:p.Lys5108Met
XM_011541108.1:c.15476A>T	XP_011539410.1:p.Lys5159Met
XM_011541109.1:c.15473A>T	XP_011539411.1:p.Lys5158Met
XM_011541110.1:c.15473A>T	XP_011539412.1:p.Lys5158Met
XM_011541111.1:c.15473A>T	XP_011539413.1:p.Lys5158Met
XM_011541112.1:c.15461A>T	XP_011539414.1:p.Lys5154Met
XM_011541113.1:c.15458A>T	XP_011539415.1:p.Lys5153Met
XM_011541114.1:c.15458A>T	XP_011539416.1:p.Lys5153Met
XM_011541115.1:c.15452A>T	XP_011539417.1:p.Lys5151Met
XM_011541116.1:c.15443A>T	XP_011539418.1:p.Lys5148Met
XM_011541117.1:c.15392A>T	XP_011539419.1:p.Lys5131Met
XM_011541118.1:c.15389A>T	XP_011539420.1:p.Lys5130Met
XM_011541119.1:c.15356A>T	XP_011539421.1:p.Lys5119Met
XM_011541120.1:c.15353A>T	XP_011539422.1:p.Lys5118Met
XM_011541121.1:c.15320A>T	XP_011539423.1:p.Lys5107Met
XM_011541108.3:c.15590A>T	XP_011539410.2:p.Lys5197Met
XM_011541109.3:c.15587A>T	XP_011539411.2:p.Lys5196Met
XM_011541110.3:c.15587A>T	XP_011539412.2:p.Lys5196Met
XM_011541111.3:c.15587A>T	XP_011539413.2:p.Lys5196Met
XM_011541112.3:c.15575A>T	XP_011539414.2:p.Lys5192Met
XM_011541113.3:c.15572A>T	XP_011539415.2:p.Lys5191Met
XM_011541114.3:c.15572A>T	XP_011539416.2:p.Lys5191Met
XM_011541115.3:c.15566A>T	XP_011539417.2:p.Lys5189Met
XM_011541116.3:c.15557A>T	XP_011539418.2:p.Lys5186Met
XM_011541117.3:c.15506A>T	XP_011539419.2:p.Lys5169Met
XM_011541118.3:c.15503A>T	XP_011539420.2:p.Lys5168Met
XM_011541119.3:c.15470A>T	XP_011539421.2:p.Lys5157Met
XM_011541120.3:c.15467A>T	XP_011539422.2:p.Lys5156Met
XM_011541121.3:c.15434A>T	XP_011539423.2:p.Lys5145Met
XM_017000822.2:c.15569A>T	XP_016856311.2:p.Lys5190Met
XM_017000823.2:c.15542A>T	XP_016856312.2:p.Lys5181Met
XM_017000824.2:c.15488A>T	XP_016856313.2:p.Lys5163Met
XM_017000825.2:c.15473A>T	XP_016856314.2:p.Lys5158Met
XM_017000826.2:c.15470A>T	XP_016856315.2:p.Lys5157Met
XM_017000827.2:c.15455A>T	XP_016856316.2:p.Lys5152Met
XM_017000828.2:c.15431A>T	XP_016856317.2:p.Lys5144Met
XM_017000829.2:c.15383A>T	XP_016856318.2:p.Lys5128Met
XM_017000830.2:c.15332A>T	XP_016856319.2:p.Lys5111Met
NM_020765.3:c.15323A>T MANE Select	NP_065816.2:p.Lys5108Met