Canonical Allele Identifier: CA390811419
Gene: UBR7 HGNC NCBI

Linked Data

dbSNP Id: rs1321827958

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218715A>G , CM000676.2:g.93218715A>G GRCh38
NC_000014.8:g.93685061A>G , CM000676.1:g.93685061A>G GRCh37
NC_000014.7:g.92754814A>G NCBI36
NG_051089.1:g.16660A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.790A>G MANE Select ENSP00000013070.6:p.Ser264Gly
ENST00000013070.10:c.790A>G ENSP00000013070.6:p.Ser264Gly
ENST00000416753.5:c.562A>G ENSP00000391706.2:p.Ser188Gly
ENST00000553674.1:c.*491A>G ENSP00000450470.1:n.*491A>G
ENST00000553857.5:c.378+3434A>G
ENST00000555329.1:c.35A>G
NM_175748.3:c.790A>G NP_786924.2:p.Ser264Gly
NR_038150.1:n.892A>G
NM_175748.4:c.790A>G MANE Select NP_786924.2:p.Ser264Gly
NR_038150.2:n.692A>G