Canonical Allele Identifier: CA2809539951
Gene: RPL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42998656del , CM000679.2:g.42998656del GRCh38
NC_000017.10:g.41150673del , CM000679.1:g.41150673del GRCh37
NC_000017.9:g.38404199del NCBI36
NG_053099.1:g.5384del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.-2-93del MANE Select ENSP00000253788.5:n.-2-93del
ENST00000589913.6:c.-95del ENSP00000464813.1:n.-95del
ENST00000253788.9:c.-2-93del ENSP00000253788.4:n.-2-93del
ENST00000587478.1:n.54-93del
ENST00000588830.1:c.-2-93del ENSP00000468468.1:n.-2-93del
ENST00000589037.5:c.-2-93del ENSP00000467587.1:n.-2-93del
ENST00000589913.5:c.-95del ENSP00000464813.1:n.-95del
ENST00000593262.1:n.238del
NM_000988.3:c.-2-93del NP_000979.1:n.-2-93del
NM_000988.5:c.-2-93del MANE Select NP_000979.1:n.-2-93del
NM_001349921.1:c.-2-93del NP_001336850.1:n.-2-93del
NM_001349922.1:c.-95del NP_001336851.1:n.-95del
NR_146327.1:n.82-93del
NM_001349921.2:c.-2-93del NP_001336850.1:n.-2-93del
NM_001349922.2:c.-95del NP_001336851.1:n.-95del
NR_146327.2:n.54-93del