Canonical Allele Identifier: CA338748080

Gene: UBR4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15313A>T MANE Select	ENSP00000364403.3:p.Asn5105Tyr
ENST00000375224.1:c.2434A>T	ENSP00000364372.1:p.Asn812Tyr
ENST00000375225.7:c.538A>T	ENSP00000364373.3:p.Asn180Tyr
ENST00000375254.7:c.15313A>T	ENSP00000364403.3:p.Asn5105Tyr
ENST00000459947.5:n.3320A>T
NM_020765.2:c.15313A>T	NP_065816.2:p.Asn5105Tyr
XM_011541108.1:c.15466A>T	XP_011539410.1:p.Asn5156Tyr
XM_011541109.1:c.15463A>T	XP_011539411.1:p.Asn5155Tyr
XM_011541110.1:c.15463A>T	XP_011539412.1:p.Asn5155Tyr
XM_011541111.1:c.15463A>T	XP_011539413.1:p.Asn5155Tyr
XM_011541112.1:c.15451A>T	XP_011539414.1:p.Asn5151Tyr
XM_011541113.1:c.15448A>T	XP_011539415.1:p.Asn5150Tyr
XM_011541114.1:c.15448A>T	XP_011539416.1:p.Asn5150Tyr
XM_011541115.1:c.15442A>T	XP_011539417.1:p.Asn5148Tyr
XM_011541116.1:c.15433A>T	XP_011539418.1:p.Asn5145Tyr
XM_011541117.1:c.15382A>T	XP_011539419.1:p.Asn5128Tyr
XM_011541118.1:c.15379A>T	XP_011539420.1:p.Asn5127Tyr
XM_011541119.1:c.15346A>T	XP_011539421.1:p.Asn5116Tyr
XM_011541120.1:c.15343A>T	XP_011539422.1:p.Asn5115Tyr
XM_011541121.1:c.15310A>T	XP_011539423.1:p.Asn5104Tyr
XM_011541108.3:c.15580A>T	XP_011539410.2:p.Asn5194Tyr
XM_011541109.3:c.15577A>T	XP_011539411.2:p.Asn5193Tyr
XM_011541110.3:c.15577A>T	XP_011539412.2:p.Asn5193Tyr
XM_011541111.3:c.15577A>T	XP_011539413.2:p.Asn5193Tyr
XM_011541112.3:c.15565A>T	XP_011539414.2:p.Asn5189Tyr
XM_011541113.3:c.15562A>T	XP_011539415.2:p.Asn5188Tyr
XM_011541114.3:c.15562A>T	XP_011539416.2:p.Asn5188Tyr
XM_011541115.3:c.15556A>T	XP_011539417.2:p.Asn5186Tyr
XM_011541116.3:c.15547A>T	XP_011539418.2:p.Asn5183Tyr
XM_011541117.3:c.15496A>T	XP_011539419.2:p.Asn5166Tyr
XM_011541118.3:c.15493A>T	XP_011539420.2:p.Asn5165Tyr
XM_011541119.3:c.15460A>T	XP_011539421.2:p.Asn5154Tyr
XM_011541120.3:c.15457A>T	XP_011539422.2:p.Asn5153Tyr
XM_011541121.3:c.15424A>T	XP_011539423.2:p.Asn5142Tyr
XM_017000822.2:c.15559A>T	XP_016856311.2:p.Asn5187Tyr
XM_017000823.2:c.15532A>T	XP_016856312.2:p.Asn5178Tyr
XM_017000824.2:c.15478A>T	XP_016856313.2:p.Asn5160Tyr
XM_017000825.2:c.15463A>T	XP_016856314.2:p.Asn5155Tyr
XM_017000826.2:c.15460A>T	XP_016856315.2:p.Asn5154Tyr
XM_017000827.2:c.15445A>T	XP_016856316.2:p.Asn5149Tyr
XM_017000828.2:c.15421A>T	XP_016856317.2:p.Asn5141Tyr
XM_017000829.2:c.15373A>T	XP_016856318.2:p.Asn5125Tyr
XM_017000830.2:c.15322A>T	XP_016856319.2:p.Asn5108Tyr
NM_020765.3:c.15313A>T MANE Select	NP_065816.2:p.Asn5105Tyr