Canonical Allele Identifier: CA656362032

Gene: RPL27

Linked Data

• COSMIC: COSN23250522

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999173_42999174insC , CM000679.2:g.42999173_42999174insC	GRCh38
NC_000017.10:g.41151190_41151191insC , CM000679.1:g.41151190_41151191insC	GRCh37
NC_000017.9:g.38404716_38404717insC	NCBI36
NG_053099.1:g.5901_5902insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+342_81+343insC MANE Select	ENSP00000253788.5:n.81+342_81+343insC
ENST00000589913.6:c.81+342_81+343insC	ENSP00000464813.1:n.81+342_81+343insC
ENST00000590864.2:c.82-13_82-12insC	ENSP00000467939.2:n.82-13_82-12insC
ENST00000253788.9:c.81+342_81+343insC	ENSP00000253788.4:n.81+342_81+343insC
ENST00000586277.5:c.104+261_104+262insC
ENST00000587478.1:n.478_479insC
ENST00000588830.1:c.81+342_81+343insC	ENSP00000468468.1:n.81+342_81+343insC
ENST00000589037.5:c.81+342_81+343insC	ENSP00000467587.1:n.81+342_81+343insC
ENST00000589913.5:c.81+342_81+343insC	ENSP00000464813.1:n.81+342_81+343insC
ENST00000593262.1:n.755_756insC
NM_000988.3:c.81+342_81+343insC	NP_000979.1:n.81+342_81+343insC
NM_000988.5:c.81+342_81+343insC MANE Select	NP_000979.1:n.81+342_81+343insC
NM_001349921.1:c.81+342_81+343insC	NP_001336850.1:n.81+342_81+343insC
NM_001349922.1:c.81+342_81+343insC	NP_001336851.1:n.81+342_81+343insC
NR_146327.1:n.164+342_164+343insC
NM_001349921.2:c.81+342_81+343insC	NP_001336850.1:n.81+342_81+343insC
NM_001349922.2:c.81+342_81+343insC	NP_001336851.1:n.81+342_81+343insC
NR_146327.2:n.136+342_136+343insC