Canonical Allele Identifier: CA2260738983
Gene: RPL27 HGNC NCBI

Linked Data

dbSNP Id: rs2050331590

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42999076_42999077del , CM000679.2:g.42999076_42999077del GRCh38
NC_000017.10:g.41151093_41151094del , CM000679.1:g.41151093_41151094del GRCh37
NC_000017.9:g.38404619_38404620del NCBI36
NG_053099.1:g.5804_5805del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.81+245_81+246del MANE Select ENSP00000253788.5:n.81+245_81+246del
ENST00000589913.6:c.81+245_81+246del ENSP00000464813.1:n.81+245_81+246del
ENST00000590864.2:c.82-110_82-109del ENSP00000467939.2:n.82-110_82-109del
ENST00000253788.9:c.81+245_81+246del ENSP00000253788.4:n.81+245_81+246del
ENST00000586277.5:c.104+164_104+165del
ENST00000587478.1:n.381_382del
ENST00000588830.1:c.81+245_81+246del ENSP00000468468.1:n.81+245_81+246del
ENST00000589037.5:c.81+245_81+246del ENSP00000467587.1:n.81+245_81+246del
ENST00000589913.5:c.81+245_81+246del ENSP00000464813.1:n.81+245_81+246del
ENST00000593262.1:n.658_659del
NM_000988.3:c.81+245_81+246del NP_000979.1:n.81+245_81+246del
NM_000988.5:c.81+245_81+246del MANE Select NP_000979.1:n.81+245_81+246del
NM_001349921.1:c.81+245_81+246del NP_001336850.1:n.81+245_81+246del
NM_001349922.1:c.81+245_81+246del NP_001336851.1:n.81+245_81+246del
NR_146327.1:n.164+245_164+246del
NM_001349921.2:c.81+245_81+246del NP_001336850.1:n.81+245_81+246del
NM_001349922.2:c.81+245_81+246del NP_001336851.1:n.81+245_81+246del
NR_146327.2:n.136+245_136+246del