Canonical Allele Identifier: CA2155441076
Gene: UBR7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218686_93218688delinsAGC , CM000676.2:g.93218686_93218688delinsAGC GRCh38
NC_000014.8:g.93685032_93685034delinsAGC , CM000676.1:g.93685032_93685034delinsAGC GRCh37
NC_000014.7:g.92754785_92754787delinsAGC NCBI36
NG_051089.1:g.16631_16633delinsAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.761_763delinsAGC MANE Select ENSP00000013070.6:p.Glu254=
ENST00000013070.10:c.761_763delinsAGC ENSP00000013070.6:p.Glu254=
ENST00000416753.5:c.533_535delinsAGC ENSP00000391706.2:p.Glu178=
ENST00000553674.1:c.*462_*464delinsAGC ENSP00000450470.1:n.*462_*464delinsAGC
ENST00000553857.5:c.378+3405_378+3407delinsAGC
ENST00000555329.1:c.6_8delinsAGC
NM_175748.3:c.761_763delinsAGC NP_786924.2:p.Glu254=
NR_038150.1:n.863_865delinsAGC
NM_175748.4:c.761_763delinsAGC MANE Select NP_786924.2:p.Glu254=
NR_038150.2:n.663_665delinsAGC
Search 100 bp 5'
Search 100 bp 3'