Canonical Allele Identifier: CA2155441037
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218587A= , CM000676.2:g.93218587A= GRCh38
NC_000014.8:g.93684933A= , CM000676.1:g.93684933A= GRCh37
NC_000014.7:g.92754686A= NCBI36
NG_051089.1:g.16532A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.662A= MANE Select ENSP00000013070.6:p.Gln221=
ENST00000013070.10:c.662A= ENSP00000013070.6:p.Gln221=
ENST00000416753.5:c.434A= ENSP00000391706.2:p.Gln145=
ENST00000553674.1:c.*363A= ENSP00000450470.1:n.*363A=
ENST00000553857.5:c.378+3306A=
ENST00000556871.5:c.371A= ENSP00000451022.1:p.Gln124=
NM_175748.3:c.662A= NP_786924.2:p.Gln221=
NR_038150.1:n.764A=
NM_175748.4:c.662A= MANE Select NP_786924.2:p.Gln221=
NR_038150.2:n.564A=