Canonical Allele Identifier: CA338748084

Gene: UBR4

Linked Data

• MyVariant Identifiers: chr1:g.19404481T>G (hg19) ; chr1:g.19077987T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.19077987T>G , CM000663.2:g.19077987T>G	GRCh38
NC_000001.10:g.19404481T>G , CM000663.1:g.19404481T>G	GRCh37
NC_000001.9:g.19277068T>G	NCBI36
NG_027669.1:g.137266A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15313A>C MANE Select	ENSP00000364403.3:p.Asn5105His
ENST00000375224.1:c.2434A>C	ENSP00000364372.1:p.Asn812His
ENST00000375225.7:c.538A>C	ENSP00000364373.3:p.Asn180His
ENST00000375254.7:c.15313A>C	ENSP00000364403.3:p.Asn5105His
ENST00000459947.5:n.3320A>C
NM_020765.2:c.15313A>C	NP_065816.2:p.Asn5105His
XM_011541108.1:c.15466A>C	XP_011539410.1:p.Asn5156His
XM_011541109.1:c.15463A>C	XP_011539411.1:p.Asn5155His
XM_011541110.1:c.15463A>C	XP_011539412.1:p.Asn5155His
XM_011541111.1:c.15463A>C	XP_011539413.1:p.Asn5155His
XM_011541112.1:c.15451A>C	XP_011539414.1:p.Asn5151His
XM_011541113.1:c.15448A>C	XP_011539415.1:p.Asn5150His
XM_011541114.1:c.15448A>C	XP_011539416.1:p.Asn5150His
XM_011541115.1:c.15442A>C	XP_011539417.1:p.Asn5148His
XM_011541116.1:c.15433A>C	XP_011539418.1:p.Asn5145His
XM_011541117.1:c.15382A>C	XP_011539419.1:p.Asn5128His
XM_011541118.1:c.15379A>C	XP_011539420.1:p.Asn5127His
XM_011541119.1:c.15346A>C	XP_011539421.1:p.Asn5116His
XM_011541120.1:c.15343A>C	XP_011539422.1:p.Asn5115His
XM_011541121.1:c.15310A>C	XP_011539423.1:p.Asn5104His
XM_011541108.3:c.15580A>C	XP_011539410.2:p.Asn5194His
XM_011541109.3:c.15577A>C	XP_011539411.2:p.Asn5193His
XM_011541110.3:c.15577A>C	XP_011539412.2:p.Asn5193His
XM_011541111.3:c.15577A>C	XP_011539413.2:p.Asn5193His
XM_011541112.3:c.15565A>C	XP_011539414.2:p.Asn5189His
XM_011541113.3:c.15562A>C	XP_011539415.2:p.Asn5188His
XM_011541114.3:c.15562A>C	XP_011539416.2:p.Asn5188His
XM_011541115.3:c.15556A>C	XP_011539417.2:p.Asn5186His
XM_011541116.3:c.15547A>C	XP_011539418.2:p.Asn5183His
XM_011541117.3:c.15496A>C	XP_011539419.2:p.Asn5166His
XM_011541118.3:c.15493A>C	XP_011539420.2:p.Asn5165His
XM_011541119.3:c.15460A>C	XP_011539421.2:p.Asn5154His
XM_011541120.3:c.15457A>C	XP_011539422.2:p.Asn5153His
XM_011541121.3:c.15424A>C	XP_011539423.2:p.Asn5142His
XM_017000822.2:c.15559A>C	XP_016856311.2:p.Asn5187His
XM_017000823.2:c.15532A>C	XP_016856312.2:p.Asn5178His
XM_017000824.2:c.15478A>C	XP_016856313.2:p.Asn5160His
XM_017000825.2:c.15463A>C	XP_016856314.2:p.Asn5155His
XM_017000826.2:c.15460A>C	XP_016856315.2:p.Asn5154His
XM_017000827.2:c.15445A>C	XP_016856316.2:p.Asn5149His
XM_017000828.2:c.15421A>C	XP_016856317.2:p.Asn5141His
XM_017000829.2:c.15373A>C	XP_016856318.2:p.Asn5125His
XM_017000830.2:c.15322A>C	XP_016856319.2:p.Asn5108His
NM_020765.3:c.15313A>C MANE Select	NP_065816.2:p.Asn5105His