Canonical Allele Identifier: CA2626239157
Gene: UBR7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218459G>T , CM000676.2:g.93218459G>T GRCh38
NC_000014.8:g.93684805G>T , CM000676.1:g.93684805G>T GRCh37
NC_000014.7:g.92754558G>T NCBI36
NG_051089.1:g.16404G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-68G>T MANE Select ENSP00000013070.6:n.602-68G>T
ENST00000013070.10:c.602-68G>T ENSP00000013070.6:n.602-68G>T
ENST00000416753.5:c.374-68G>T ENSP00000391706.2:n.374-68G>T
ENST00000553674.1:c.*303-68G>T ENSP00000450470.1:n.*303-68G>T
ENST00000553857.5:c.378+3178G>T
ENST00000554232.5:c.506-68G>T ENSP00000450645.1:n.506-68G>T
ENST00000556871.5:c.311-68G>T ENSP00000451022.1:n.311-68G>T
ENST00000557048.1:n.511-68G>T
NM_175748.3:c.602-68G>T NP_786924.2:n.602-68G>T
NR_038150.1:n.704-68G>T
NM_175748.4:c.602-68G>T MANE Select NP_786924.2:n.602-68G>T
NR_038150.2:n.504-68G>T