Canonical Allele Identifier: CA2260739006

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999141_42999143delinsCAT , CM000679.2:g.42999141_42999143delinsCAT	GRCh38
NC_000017.10:g.41151158_41151160delinsCAT , CM000679.1:g.41151158_41151160delinsCAT	GRCh37
NC_000017.9:g.38404684_38404686delinsCAT	NCBI36
NG_053099.1:g.5869_5871delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+310_81+312delinsCAT MANE Select	ENSP00000253788.5:n.81+310_81+312delinsCAT
ENST00000589913.6:c.81+310_81+312delinsCAT	ENSP00000464813.1:n.81+310_81+312delinsCAT
ENST00000590864.2:c.82-45_82-43delinsCAT	ENSP00000467939.2:n.82-45_82-43delinsCAT
ENST00000253788.9:c.81+310_81+312delinsCAT	ENSP00000253788.4:n.81+310_81+312delinsCAT
ENST00000586277.5:c.104+229_104+231delinsCAT
ENST00000587478.1:n.446_448delinsCAT
ENST00000588830.1:c.81+310_81+312delinsCAT	ENSP00000468468.1:n.81+310_81+312delinsCAT
ENST00000589037.5:c.81+310_81+312delinsCAT	ENSP00000467587.1:n.81+310_81+312delinsCAT
ENST00000589913.5:c.81+310_81+312delinsCAT	ENSP00000464813.1:n.81+310_81+312delinsCAT
ENST00000593262.1:n.723_725delinsCAT
NM_000988.3:c.81+310_81+312delinsCAT	NP_000979.1:n.81+310_81+312delinsCAT
NM_000988.5:c.81+310_81+312delinsCAT MANE Select	NP_000979.1:n.81+310_81+312delinsCAT
NM_001349921.1:c.81+310_81+312delinsCAT	NP_001336850.1:n.81+310_81+312delinsCAT
NM_001349922.1:c.81+310_81+312delinsCAT	NP_001336851.1:n.81+310_81+312delinsCAT
NR_146327.1:n.164+310_164+312delinsCAT
NM_001349921.2:c.81+310_81+312delinsCAT	NP_001336850.1:n.81+310_81+312delinsCAT
NM_001349922.2:c.81+310_81+312delinsCAT	NP_001336851.1:n.81+310_81+312delinsCAT
NR_146327.2:n.136+310_136+312delinsCAT