Canonical Allele Identifier: CA2155441077
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218690G= , CM000676.2:g.93218690G= GRCh38
NC_000014.8:g.93685036G= , CM000676.1:g.93685036G= GRCh37
NC_000014.7:g.92754789G= NCBI36
NG_051089.1:g.16635G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.765G= MANE Select ENSP00000013070.6:p.Gln255=
ENST00000013070.10:c.765G= ENSP00000013070.6:p.Gln255=
ENST00000416753.5:c.537G= ENSP00000391706.2:p.Gln179=
ENST00000553674.1:c.*466G= ENSP00000450470.1:n.*466G=
ENST00000553857.5:c.378+3409G=
ENST00000555329.1:c.10G=
NM_175748.3:c.765G= NP_786924.2:p.Gln255=
NR_038150.1:n.867G=
NM_175748.4:c.765G= MANE Select NP_786924.2:p.Gln255=
NR_038150.2:n.667G=