Canonical Allele Identifier: CA2260738959

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999032_42999035delinsCCTT , CM000679.2:g.42999032_42999035delinsCCTT	GRCh38
NC_000017.10:g.41151049_41151052delinsCCTT , CM000679.1:g.41151049_41151052delinsCCTT	GRCh37
NC_000017.9:g.38404575_38404578delinsCCTT	NCBI36
NG_053099.1:g.5760_5763delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+201_81+204delinsCCTT MANE Select	ENSP00000253788.5:n.81+201_81+204delinsCCTT
ENST00000589913.6:c.81+201_81+204delinsCCTT	ENSP00000464813.1:n.81+201_81+204delinsCCTT
ENST00000590864.2:c.82-154_82-151delinsCCTT	ENSP00000467939.2:n.82-154_82-151delinsCCTT
ENST00000253788.9:c.81+201_81+204delinsCCTT	ENSP00000253788.4:n.81+201_81+204delinsCCTT
ENST00000586277.5:c.104+120_104+123delinsCCTT
ENST00000587478.1:n.337_340delinsCCTT
ENST00000588830.1:c.81+201_81+204delinsCCTT	ENSP00000468468.1:n.81+201_81+204delinsCCTT
ENST00000589037.5:c.81+201_81+204delinsCCTT	ENSP00000467587.1:n.81+201_81+204delinsCCTT
ENST00000589913.5:c.81+201_81+204delinsCCTT	ENSP00000464813.1:n.81+201_81+204delinsCCTT
ENST00000593262.1:n.614_617delinsCCTT
NM_000988.3:c.81+201_81+204delinsCCTT	NP_000979.1:n.81+201_81+204delinsCCTT
NM_000988.5:c.81+201_81+204delinsCCTT MANE Select	NP_000979.1:n.81+201_81+204delinsCCTT
NM_001349921.1:c.81+201_81+204delinsCCTT	NP_001336850.1:n.81+201_81+204delinsCCTT
NM_001349922.1:c.81+201_81+204delinsCCTT	NP_001336851.1:n.81+201_81+204delinsCCTT
NR_146327.1:n.164+201_164+204delinsCCTT
NM_001349921.2:c.81+201_81+204delinsCCTT	NP_001336850.1:n.81+201_81+204delinsCCTT
NM_001349922.2:c.81+201_81+204delinsCCTT	NP_001336851.1:n.81+201_81+204delinsCCTT
NR_146327.2:n.136+201_136+204delinsCCTT