Canonical Allele Identifier: CA2260738696

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998551_42998552delinsGC , CM000679.2:g.42998551_42998552delinsGC	GRCh38
NC_000017.10:g.41150568_41150569delinsGC , CM000679.1:g.41150568_41150569delinsGC	GRCh37
NC_000017.9:g.38404094_38404095delinsGC	NCBI36
NG_053099.1:g.5279_5280delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+80_-3+81delinsGC MANE Select	ENSP00000253788.5:n.-3+80_-3+81delinsGC
ENST00000589913.6:c.-200_-199delinsGC	ENSP00000464813.1:n.-200_-199delinsGC
ENST00000253788.9:c.-3+80_-3+81delinsGC	ENSP00000253788.4:n.-3+80_-3+81delinsGC
ENST00000587478.1:n.53+80_53+81delinsGC
ENST00000588830.1:c.-3+80_-3+81delinsGC	ENSP00000468468.1:n.-3+80_-3+81delinsGC
ENST00000589037.5:c.-3+136_-3+137delinsGC	ENSP00000467587.1:n.-3+136_-3+137delinsGC
ENST00000589913.5:c.-200_-199delinsGC	ENSP00000464813.1:n.-200_-199delinsGC
ENST00000593262.1:n.133_134delinsGC
NM_000988.3:c.-3+80_-3+81delinsGC	NP_000979.1:n.-3+80_-3+81delinsGC
NM_000988.5:c.-3+80_-3+81delinsGC MANE Select	NP_000979.1:n.-3+80_-3+81delinsGC
NM_001349921.1:c.-3+136_-3+137delinsGC	NP_001336850.1:n.-3+136_-3+137delinsGC
NM_001349922.1:c.-200_-199delinsGC	NP_001336851.1:n.-200_-199delinsGC
NR_146327.1:n.81+80_81+81delinsGC
NM_001349921.2:c.-3+136_-3+137delinsGC	NP_001336850.1:n.-3+136_-3+137delinsGC
NM_001349922.2:c.-200_-199delinsGC	NP_001336851.1:n.-200_-199delinsGC
NR_146327.2:n.53+80_53+81delinsGC