Canonical Allele Identifier: CA2260738912

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998965_42998966delinsGT , CM000679.2:g.42998965_42998966delinsGT	GRCh38
NC_000017.10:g.41150982_41150983delinsGT , CM000679.1:g.41150982_41150983delinsGT	GRCh37
NC_000017.9:g.38404508_38404509delinsGT	NCBI36
NG_053099.1:g.5693_5694delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+134_81+135delinsGT MANE Select	ENSP00000253788.5:n.81+134_81+135delinsGT
ENST00000589913.6:c.81+134_81+135delinsGT	ENSP00000464813.1:n.81+134_81+135delinsGT
ENST00000590864.2:c.81+134_81+135delinsGT	ENSP00000467939.2:n.81+134_81+135delinsGT
ENST00000253788.9:c.81+134_81+135delinsGT	ENSP00000253788.4:n.81+134_81+135delinsGT
ENST00000586277.5:c.104+53_104+54delinsGT
ENST00000587478.1:n.270_271delinsGT
ENST00000588830.1:c.81+134_81+135delinsGT	ENSP00000468468.1:n.81+134_81+135delinsGT
ENST00000589037.5:c.81+134_81+135delinsGT	ENSP00000467587.1:n.81+134_81+135delinsGT
ENST00000589913.5:c.81+134_81+135delinsGT	ENSP00000464813.1:n.81+134_81+135delinsGT
ENST00000593262.1:n.547_548delinsGT
NM_000988.3:c.81+134_81+135delinsGT	NP_000979.1:n.81+134_81+135delinsGT
NM_000988.5:c.81+134_81+135delinsGT MANE Select	NP_000979.1:n.81+134_81+135delinsGT
NM_001349921.1:c.81+134_81+135delinsGT	NP_001336850.1:n.81+134_81+135delinsGT
NM_001349922.1:c.81+134_81+135delinsGT	NP_001336851.1:n.81+134_81+135delinsGT
NR_146327.1:n.164+134_164+135delinsGT
NM_001349921.2:c.81+134_81+135delinsGT	NP_001336850.1:n.81+134_81+135delinsGT
NM_001349922.2:c.81+134_81+135delinsGT	NP_001336851.1:n.81+134_81+135delinsGT
NR_146327.2:n.136+134_136+135delinsGT