Canonical Allele Identifier: CA338748138

Gene: UBR4

Linked Data

• COSMIC: COSM424878 ; COSM4815148 ; COSM4815149 ; COSM4815150 ; COSM5832396
• MyVariant Identifiers: chr1:g.19404496C>G (hg19) ; chr1:g.19078002C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19078002C>G , CM000663.2:g.19078002C>G	GRCh38
NC_000001.10:g.19404496C>G , CM000663.1:g.19404496C>G	GRCh37
NC_000001.9:g.19277083C>G	NCBI36
NG_027669.1:g.137251G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15298G>C MANE Select	ENSP00000364403.3:p.Val5100Leu
ENST00000375224.1:c.2419G>C	ENSP00000364372.1:p.Val807Leu
ENST00000375225.7:c.523G>C	ENSP00000364373.3:p.Val175Leu
ENST00000375254.7:c.15298G>C	ENSP00000364403.3:p.Val5100Leu
ENST00000459947.5:n.3305G>C
NM_020765.2:c.15298G>C	NP_065816.2:p.Val5100Leu
XM_011541108.1:c.15451G>C	XP_011539410.1:p.Val5151Leu
XM_011541109.1:c.15448G>C	XP_011539411.1:p.Val5150Leu
XM_011541110.1:c.15448G>C	XP_011539412.1:p.Val5150Leu
XM_011541111.1:c.15448G>C	XP_011539413.1:p.Val5150Leu
XM_011541112.1:c.15436G>C	XP_011539414.1:p.Val5146Leu
XM_011541113.1:c.15433G>C	XP_011539415.1:p.Val5145Leu
XM_011541114.1:c.15433G>C	XP_011539416.1:p.Val5145Leu
XM_011541115.1:c.15427G>C	XP_011539417.1:p.Val5143Leu
XM_011541116.1:c.15418G>C	XP_011539418.1:p.Val5140Leu
XM_011541117.1:c.15367G>C	XP_011539419.1:p.Val5123Leu
XM_011541118.1:c.15364G>C	XP_011539420.1:p.Val5122Leu
XM_011541119.1:c.15331G>C	XP_011539421.1:p.Val5111Leu
XM_011541120.1:c.15328G>C	XP_011539422.1:p.Val5110Leu
XM_011541121.1:c.15295G>C	XP_011539423.1:p.Val5099Leu
XM_011541108.3:c.15565G>C	XP_011539410.2:p.Val5189Leu
XM_011541109.3:c.15562G>C	XP_011539411.2:p.Val5188Leu
XM_011541110.3:c.15562G>C	XP_011539412.2:p.Val5188Leu
XM_011541111.3:c.15562G>C	XP_011539413.2:p.Val5188Leu
XM_011541112.3:c.15550G>C	XP_011539414.2:p.Val5184Leu
XM_011541113.3:c.15547G>C	XP_011539415.2:p.Val5183Leu
XM_011541114.3:c.15547G>C	XP_011539416.2:p.Val5183Leu
XM_011541115.3:c.15541G>C	XP_011539417.2:p.Val5181Leu
XM_011541116.3:c.15532G>C	XP_011539418.2:p.Val5178Leu
XM_011541117.3:c.15481G>C	XP_011539419.2:p.Val5161Leu
XM_011541118.3:c.15478G>C	XP_011539420.2:p.Val5160Leu
XM_011541119.3:c.15445G>C	XP_011539421.2:p.Val5149Leu
XM_011541120.3:c.15442G>C	XP_011539422.2:p.Val5148Leu
XM_011541121.3:c.15409G>C	XP_011539423.2:p.Val5137Leu
XM_017000822.2:c.15544G>C	XP_016856311.2:p.Val5182Leu
XM_017000823.2:c.15517G>C	XP_016856312.2:p.Val5173Leu
XM_017000824.2:c.15463G>C	XP_016856313.2:p.Val5155Leu
XM_017000825.2:c.15448G>C	XP_016856314.2:p.Val5150Leu
XM_017000826.2:c.15445G>C	XP_016856315.2:p.Val5149Leu
XM_017000827.2:c.15430G>C	XP_016856316.2:p.Val5144Leu
XM_017000828.2:c.15406G>C	XP_016856317.2:p.Val5136Leu
XM_017000829.2:c.15358G>C	XP_016856318.2:p.Val5120Leu
XM_017000830.2:c.15307G>C	XP_016856319.2:p.Val5103Leu
NM_020765.3:c.15298G>C MANE Select	NP_065816.2:p.Val5100Leu