Canonical Allele Identifier: CA2155440955
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218418A= , CM000676.2:g.93218418A= GRCh38
NC_000014.8:g.93684764A= , CM000676.1:g.93684764A= GRCh37
NC_000014.7:g.92754517A= NCBI36
NG_051089.1:g.16363A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-109A= MANE Select ENSP00000013070.6:n.602-109A=
ENST00000013070.10:c.602-109A= ENSP00000013070.6:n.602-109A=
ENST00000416753.5:c.374-109A= ENSP00000391706.2:n.374-109A=
ENST00000553674.1:c.*303-109A= ENSP00000450470.1:n.*303-109A=
ENST00000553857.5:c.378+3137A=
ENST00000554232.5:c.506-109A= ENSP00000450645.1:n.506-109A=
ENST00000556871.5:c.311-109A= ENSP00000451022.1:n.311-109A=
ENST00000557048.1:n.511-109A=
NM_175748.3:c.602-109A= NP_786924.2:n.602-109A=
NR_038150.1:n.704-109A=
NM_175748.4:c.602-109A= MANE Select NP_786924.2:n.602-109A=
NR_038150.2:n.504-109A=