Canonical Allele Identifier: CA2155441062
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218661G= , CM000676.2:g.93218661G= GRCh38
NC_000014.8:g.93685007G= , CM000676.1:g.93685007G= GRCh37
NC_000014.7:g.92754760G= NCBI36
NG_051089.1:g.16606G=

Transcript Alleles

HGVS Amino-acid change
ENST00000013070.11:c.736G= MANE Select ENSP00000013070.6:p.Asp246=
ENST00000013070.10:c.736G= ENSP00000013070.6:p.Asp246=
ENST00000416753.5:c.508G= ENSP00000391706.2:p.Asp170=
ENST00000553674.1:c.*437G= ENSP00000450470.1:n.*437G=
ENST00000553857.5:c.378+3380G=
ENST00000556871.5:c.445G= ENSP00000451022.1:p.Asp149=
NM_175748.3:c.736G= NP_786924.2:p.Asp246=
NR_038150.1:n.838G=
NM_175748.4:c.736G= MANE Select NP_786924.2:p.Asp246=
NR_038150.2:n.638G=