Canonical Allele Identifier: CA2260738994
Gene: RPL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42999106_42999117delinsTTTCAGGTATTG , CM000679.2:g.42999106_42999117delinsTTTCAGGTATTG GRCh38
NC_000017.10:g.41151123_41151134delinsTTTCAGGTATTG , CM000679.1:g.41151123_41151134delinsTTTCAGGTATTG GRCh37
NC_000017.9:g.38404649_38404660delinsTTTCAGGTATTG NCBI36
NG_053099.1:g.5834_5845delinsTTTCAGGTATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.81+275_81+286delinsTTTCAGGTATTG MANE Select ENSP00000253788.5:n.81+275_81+286delinsTTTCAGGTATTG
ENST00000589913.6:c.81+275_81+286delinsTTTCAGGTATTG ENSP00000464813.1:n.81+275_81+286delinsTTTCAGGTATTG
ENST00000590864.2:c.82-80_82-69delinsTTTCAGGTATTG ENSP00000467939.2:n.82-80_82-69delinsTTTCAGGTATTG
ENST00000253788.9:c.81+275_81+286delinsTTTCAGGTATTG ENSP00000253788.4:n.81+275_81+286delinsTTTCAGGTATTG
ENST00000586277.5:c.104+194_104+205delinsTTTCAGGTATTG
ENST00000587478.1:n.411_422delinsTTTCAGGTATTG
ENST00000588830.1:c.81+275_81+286delinsTTTCAGGTATTG ENSP00000468468.1:n.81+275_81+286delinsTTTCAGGTATTG
ENST00000589037.5:c.81+275_81+286delinsTTTCAGGTATTG ENSP00000467587.1:n.81+275_81+286delinsTTTCAGGTATTG
ENST00000589913.5:c.81+275_81+286delinsTTTCAGGTATTG ENSP00000464813.1:n.81+275_81+286delinsTTTCAGGTATTG
ENST00000593262.1:n.688_699delinsTTTCAGGTATTG
NM_000988.3:c.81+275_81+286delinsTTTCAGGTATTG NP_000979.1:n.81+275_81+286delinsTTTCAGGTATTG
NM_000988.5:c.81+275_81+286delinsTTTCAGGTATTG MANE Select NP_000979.1:n.81+275_81+286delinsTTTCAGGTATTG
NM_001349921.1:c.81+275_81+286delinsTTTCAGGTATTG NP_001336850.1:n.81+275_81+286delinsTTTCAGGTATTG
NM_001349922.1:c.81+275_81+286delinsTTTCAGGTATTG NP_001336851.1:n.81+275_81+286delinsTTTCAGGTATTG
NR_146327.1:n.164+275_164+286delinsTTTCAGGTATTG
NM_001349921.2:c.81+275_81+286delinsTTTCAGGTATTG NP_001336850.1:n.81+275_81+286delinsTTTCAGGTATTG
NM_001349922.2:c.81+275_81+286delinsTTTCAGGTATTG NP_001336851.1:n.81+275_81+286delinsTTTCAGGTATTG
NR_146327.2:n.136+275_136+286delinsTTTCAGGTATTG