Canonical Allele Identifier: CA2155440909
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218341A= , CM000676.2:g.93218341A= GRCh38
NC_000014.8:g.93684687A= , CM000676.1:g.93684687A= GRCh37
NC_000014.7:g.92754440A= NCBI36
NG_051089.1:g.16286A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-186A= MANE Select ENSP00000013070.6:n.602-186A=
ENST00000013070.10:c.602-186A= ENSP00000013070.6:n.602-186A=
ENST00000416753.5:c.374-186A= ENSP00000391706.2:n.374-186A=
ENST00000553674.1:c.*303-186A= ENSP00000450470.1:n.*303-186A=
ENST00000553857.5:c.378+3060A=
ENST00000554232.5:c.506-186A= ENSP00000450645.1:n.506-186A=
ENST00000556871.5:c.311-186A= ENSP00000451022.1:n.311-186A=
ENST00000557048.1:n.511-186A=
NM_175748.3:c.602-186A= NP_786924.2:n.602-186A=
NR_038150.1:n.704-186A=
NM_175748.4:c.602-186A= MANE Select NP_786924.2:n.602-186A=
NR_038150.2:n.504-186A=