Canonical Allele Identifier: CA338748069

Gene: UBR4

Linked Data

• dbSNP Id: rs1362080383
• gnomAD v2: 1-19404478-T-C
• gnomAD v4: 1-19077984-T-C
• MyVariant Identifiers: chr1:g.19404478T>C (hg19) ; chr1:g.19077984T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077984T>C , CM000663.2:g.19077984T>C	GRCh38
NC_000001.10:g.19404478T>C , CM000663.1:g.19404478T>C	GRCh37
NC_000001.9:g.19277065T>C	NCBI36
NG_027669.1:g.137269A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15316A>G MANE Select	ENSP00000364403.3:p.Met5106Val
ENST00000375224.1:c.2437A>G	ENSP00000364372.1:p.Met813Val
ENST00000375225.7:c.541A>G	ENSP00000364373.3:p.Met181Val
ENST00000375254.7:c.15316A>G	ENSP00000364403.3:p.Met5106Val
ENST00000459947.5:n.3323A>G
NM_020765.2:c.15316A>G	NP_065816.2:p.Met5106Val
XM_011541108.1:c.15469A>G	XP_011539410.1:p.Met5157Val
XM_011541109.1:c.15466A>G	XP_011539411.1:p.Met5156Val
XM_011541110.1:c.15466A>G	XP_011539412.1:p.Met5156Val
XM_011541111.1:c.15466A>G	XP_011539413.1:p.Met5156Val
XM_011541112.1:c.15454A>G	XP_011539414.1:p.Met5152Val
XM_011541113.1:c.15451A>G	XP_011539415.1:p.Met5151Val
XM_011541114.1:c.15451A>G	XP_011539416.1:p.Met5151Val
XM_011541115.1:c.15445A>G	XP_011539417.1:p.Met5149Val
XM_011541116.1:c.15436A>G	XP_011539418.1:p.Met5146Val
XM_011541117.1:c.15385A>G	XP_011539419.1:p.Met5129Val
XM_011541118.1:c.15382A>G	XP_011539420.1:p.Met5128Val
XM_011541119.1:c.15349A>G	XP_011539421.1:p.Met5117Val
XM_011541120.1:c.15346A>G	XP_011539422.1:p.Met5116Val
XM_011541121.1:c.15313A>G	XP_011539423.1:p.Met5105Val
XM_011541108.3:c.15583A>G	XP_011539410.2:p.Met5195Val
XM_011541109.3:c.15580A>G	XP_011539411.2:p.Met5194Val
XM_011541110.3:c.15580A>G	XP_011539412.2:p.Met5194Val
XM_011541111.3:c.15580A>G	XP_011539413.2:p.Met5194Val
XM_011541112.3:c.15568A>G	XP_011539414.2:p.Met5190Val
XM_011541113.3:c.15565A>G	XP_011539415.2:p.Met5189Val
XM_011541114.3:c.15565A>G	XP_011539416.2:p.Met5189Val
XM_011541115.3:c.15559A>G	XP_011539417.2:p.Met5187Val
XM_011541116.3:c.15550A>G	XP_011539418.2:p.Met5184Val
XM_011541117.3:c.15499A>G	XP_011539419.2:p.Met5167Val
XM_011541118.3:c.15496A>G	XP_011539420.2:p.Met5166Val
XM_011541119.3:c.15463A>G	XP_011539421.2:p.Met5155Val
XM_011541120.3:c.15460A>G	XP_011539422.2:p.Met5154Val
XM_011541121.3:c.15427A>G	XP_011539423.2:p.Met5143Val
XM_017000822.2:c.15562A>G	XP_016856311.2:p.Met5188Val
XM_017000823.2:c.15535A>G	XP_016856312.2:p.Met5179Val
XM_017000824.2:c.15481A>G	XP_016856313.2:p.Met5161Val
XM_017000825.2:c.15466A>G	XP_016856314.2:p.Met5156Val
XM_017000826.2:c.15463A>G	XP_016856315.2:p.Met5155Val
XM_017000827.2:c.15448A>G	XP_016856316.2:p.Met5150Val
XM_017000828.2:c.15424A>G	XP_016856317.2:p.Met5142Val
XM_017000829.2:c.15376A>G	XP_016856318.2:p.Met5126Val
XM_017000830.2:c.15325A>G	XP_016856319.2:p.Met5109Val
NM_020765.3:c.15316A>G MANE Select	NP_065816.2:p.Met5106Val