Canonical Allele Identifier: CA2155440996
Gene: UBR7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218496T= , CM000676.2:g.93218496T= GRCh38
NC_000014.8:g.93684842T= , CM000676.1:g.93684842T= GRCh37
NC_000014.7:g.92754595T= NCBI36
NG_051089.1:g.16441T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-31T= MANE Select ENSP00000013070.6:n.602-31T=
ENST00000013070.10:c.602-31T= ENSP00000013070.6:n.602-31T=
ENST00000416753.5:c.374-31T= ENSP00000391706.2:n.374-31T=
ENST00000553674.1:c.*303-31T= ENSP00000450470.1:n.*303-31T=
ENST00000553857.5:c.378+3215T=
ENST00000554232.5:c.506-31T= ENSP00000450645.1:n.506-31T=
ENST00000556871.5:c.311-31T= ENSP00000451022.1:n.311-31T=
ENST00000557048.1:n.511-31T=
NM_175748.3:c.602-31T= NP_786924.2:n.602-31T=
NR_038150.1:n.704-31T=
NM_175748.4:c.602-31T= MANE Select NP_786924.2:n.602-31T=
NR_038150.2:n.504-31T=
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