Canonical Allele Identifier: CA338748082

Gene: UBR4

Linked Data

• dbSNP Id: rs2076124315
• gnomAD v4: 1-19077987-T-C
• MyVariant Identifiers: chr1:g.19404481T>C (hg19) ; chr1:g.19077987T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375254.8:c.15313A>G MANE Select	ENSP00000364403.3:p.Asn5105Asp
ENST00000375224.1:c.2434A>G	ENSP00000364372.1:p.Asn812Asp
ENST00000375225.7:c.538A>G	ENSP00000364373.3:p.Asn180Asp
ENST00000375254.7:c.15313A>G	ENSP00000364403.3:p.Asn5105Asp
ENST00000459947.5:n.3320A>G
NM_020765.2:c.15313A>G	NP_065816.2:p.Asn5105Asp
XM_011541108.1:c.15466A>G	XP_011539410.1:p.Asn5156Asp
XM_011541109.1:c.15463A>G	XP_011539411.1:p.Asn5155Asp
XM_011541110.1:c.15463A>G	XP_011539412.1:p.Asn5155Asp
XM_011541111.1:c.15463A>G	XP_011539413.1:p.Asn5155Asp
XM_011541112.1:c.15451A>G	XP_011539414.1:p.Asn5151Asp
XM_011541113.1:c.15448A>G	XP_011539415.1:p.Asn5150Asp
XM_011541114.1:c.15448A>G	XP_011539416.1:p.Asn5150Asp
XM_011541115.1:c.15442A>G	XP_011539417.1:p.Asn5148Asp
XM_011541116.1:c.15433A>G	XP_011539418.1:p.Asn5145Asp
XM_011541117.1:c.15382A>G	XP_011539419.1:p.Asn5128Asp
XM_011541118.1:c.15379A>G	XP_011539420.1:p.Asn5127Asp
XM_011541119.1:c.15346A>G	XP_011539421.1:p.Asn5116Asp
XM_011541120.1:c.15343A>G	XP_011539422.1:p.Asn5115Asp
XM_011541121.1:c.15310A>G	XP_011539423.1:p.Asn5104Asp
XM_011541108.3:c.15580A>G	XP_011539410.2:p.Asn5194Asp
XM_011541109.3:c.15577A>G	XP_011539411.2:p.Asn5193Asp
XM_011541110.3:c.15577A>G	XP_011539412.2:p.Asn5193Asp
XM_011541111.3:c.15577A>G	XP_011539413.2:p.Asn5193Asp
XM_011541112.3:c.15565A>G	XP_011539414.2:p.Asn5189Asp
XM_011541113.3:c.15562A>G	XP_011539415.2:p.Asn5188Asp
XM_011541114.3:c.15562A>G	XP_011539416.2:p.Asn5188Asp
XM_011541115.3:c.15556A>G	XP_011539417.2:p.Asn5186Asp
XM_011541116.3:c.15547A>G	XP_011539418.2:p.Asn5183Asp
XM_011541117.3:c.15496A>G	XP_011539419.2:p.Asn5166Asp
XM_011541118.3:c.15493A>G	XP_011539420.2:p.Asn5165Asp
XM_011541119.3:c.15460A>G	XP_011539421.2:p.Asn5154Asp
XM_011541120.3:c.15457A>G	XP_011539422.2:p.Asn5153Asp
XM_011541121.3:c.15424A>G	XP_011539423.2:p.Asn5142Asp
XM_017000822.2:c.15559A>G	XP_016856311.2:p.Asn5187Asp
XM_017000823.2:c.15532A>G	XP_016856312.2:p.Asn5178Asp
XM_017000824.2:c.15478A>G	XP_016856313.2:p.Asn5160Asp
XM_017000825.2:c.15463A>G	XP_016856314.2:p.Asn5155Asp
XM_017000826.2:c.15460A>G	XP_016856315.2:p.Asn5154Asp
XM_017000827.2:c.15445A>G	XP_016856316.2:p.Asn5149Asp
XM_017000828.2:c.15421A>G	XP_016856317.2:p.Asn5141Asp
XM_017000829.2:c.15373A>G	XP_016856318.2:p.Asn5125Asp
XM_017000830.2:c.15322A>G	XP_016856319.2:p.Asn5108Asp
NM_020765.3:c.15313A>G MANE Select	NP_065816.2:p.Asn5105Asp