Canonical Allele Identifier: CA338748121

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404490G>C (hg19) ; chr1:g.19077996G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077996G>C , CM000663.2:g.19077996G>C	GRCh38
NC_000001.10:g.19404490G>C , CM000663.1:g.19404490G>C	GRCh37
NC_000001.9:g.19277077G>C	NCBI36
NG_027669.1:g.137257C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15304C>G MANE Select	ENSP00000364403.3:p.Leu5102Val
ENST00000375224.1:c.2425C>G	ENSP00000364372.1:p.Leu809Val
ENST00000375225.7:c.529C>G	ENSP00000364373.3:p.Leu177Val
ENST00000375254.7:c.15304C>G	ENSP00000364403.3:p.Leu5102Val
ENST00000459947.5:n.3311C>G
NM_020765.2:c.15304C>G	NP_065816.2:p.Leu5102Val
XM_011541108.1:c.15457C>G	XP_011539410.1:p.Leu5153Val
XM_011541109.1:c.15454C>G	XP_011539411.1:p.Leu5152Val
XM_011541110.1:c.15454C>G	XP_011539412.1:p.Leu5152Val
XM_011541111.1:c.15454C>G	XP_011539413.1:p.Leu5152Val
XM_011541112.1:c.15442C>G	XP_011539414.1:p.Leu5148Val
XM_011541113.1:c.15439C>G	XP_011539415.1:p.Leu5147Val
XM_011541114.1:c.15439C>G	XP_011539416.1:p.Leu5147Val
XM_011541115.1:c.15433C>G	XP_011539417.1:p.Leu5145Val
XM_011541116.1:c.15424C>G	XP_011539418.1:p.Leu5142Val
XM_011541117.1:c.15373C>G	XP_011539419.1:p.Leu5125Val
XM_011541118.1:c.15370C>G	XP_011539420.1:p.Leu5124Val
XM_011541119.1:c.15337C>G	XP_011539421.1:p.Leu5113Val
XM_011541120.1:c.15334C>G	XP_011539422.1:p.Leu5112Val
XM_011541121.1:c.15301C>G	XP_011539423.1:p.Leu5101Val
XM_011541108.3:c.15571C>G	XP_011539410.2:p.Leu5191Val
XM_011541109.3:c.15568C>G	XP_011539411.2:p.Leu5190Val
XM_011541110.3:c.15568C>G	XP_011539412.2:p.Leu5190Val
XM_011541111.3:c.15568C>G	XP_011539413.2:p.Leu5190Val
XM_011541112.3:c.15556C>G	XP_011539414.2:p.Leu5186Val
XM_011541113.3:c.15553C>G	XP_011539415.2:p.Leu5185Val
XM_011541114.3:c.15553C>G	XP_011539416.2:p.Leu5185Val
XM_011541115.3:c.15547C>G	XP_011539417.2:p.Leu5183Val
XM_011541116.3:c.15538C>G	XP_011539418.2:p.Leu5180Val
XM_011541117.3:c.15487C>G	XP_011539419.2:p.Leu5163Val
XM_011541118.3:c.15484C>G	XP_011539420.2:p.Leu5162Val
XM_011541119.3:c.15451C>G	XP_011539421.2:p.Leu5151Val
XM_011541120.3:c.15448C>G	XP_011539422.2:p.Leu5150Val
XM_011541121.3:c.15415C>G	XP_011539423.2:p.Leu5139Val
XM_017000822.2:c.15550C>G	XP_016856311.2:p.Leu5184Val
XM_017000823.2:c.15523C>G	XP_016856312.2:p.Leu5175Val
XM_017000824.2:c.15469C>G	XP_016856313.2:p.Leu5157Val
XM_017000825.2:c.15454C>G	XP_016856314.2:p.Leu5152Val
XM_017000826.2:c.15451C>G	XP_016856315.2:p.Leu5151Val
XM_017000827.2:c.15436C>G	XP_016856316.2:p.Leu5146Val
XM_017000828.2:c.15412C>G	XP_016856317.2:p.Leu5138Val
XM_017000829.2:c.15364C>G	XP_016856318.2:p.Leu5122Val
XM_017000830.2:c.15313C>G	XP_016856319.2:p.Leu5105Val
NM_020765.3:c.15304C>G MANE Select	NP_065816.2:p.Leu5102Val