Canonical Allele Identifier: CA2260738920
Gene: RPL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42998977_42998980delinsGGAA , CM000679.2:g.42998977_42998980delinsGGAA GRCh38
NC_000017.10:g.41150994_41150997delinsGGAA , CM000679.1:g.41150994_41150997delinsGGAA GRCh37
NC_000017.9:g.38404520_38404523delinsGGAA NCBI36
NG_053099.1:g.5705_5708delinsGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.81+146_81+149delinsGGAA MANE Select ENSP00000253788.5:n.81+146_81+149delinsGGAA
ENST00000589913.6:c.81+146_81+149delinsGGAA ENSP00000464813.1:n.81+146_81+149delinsGGAA
ENST00000590864.2:c.81+146_81+149delinsGGAA ENSP00000467939.2:n.81+146_81+149delinsGGAA
ENST00000253788.9:c.81+146_81+149delinsGGAA ENSP00000253788.4:n.81+146_81+149delinsGGAA
ENST00000586277.5:c.104+65_104+68delinsGGAA
ENST00000587478.1:n.282_285delinsGGAA
ENST00000588830.1:c.81+146_81+149delinsGGAA ENSP00000468468.1:n.81+146_81+149delinsGGAA
ENST00000589037.5:c.81+146_81+149delinsGGAA ENSP00000467587.1:n.81+146_81+149delinsGGAA
ENST00000589913.5:c.81+146_81+149delinsGGAA ENSP00000464813.1:n.81+146_81+149delinsGGAA
ENST00000593262.1:n.559_562delinsGGAA
NM_000988.3:c.81+146_81+149delinsGGAA NP_000979.1:n.81+146_81+149delinsGGAA
NM_000988.5:c.81+146_81+149delinsGGAA MANE Select NP_000979.1:n.81+146_81+149delinsGGAA
NM_001349921.1:c.81+146_81+149delinsGGAA NP_001336850.1:n.81+146_81+149delinsGGAA
NM_001349922.1:c.81+146_81+149delinsGGAA NP_001336851.1:n.81+146_81+149delinsGGAA
NR_146327.1:n.164+146_164+149delinsGGAA
NM_001349921.2:c.81+146_81+149delinsGGAA NP_001336850.1:n.81+146_81+149delinsGGAA
NM_001349922.2:c.81+146_81+149delinsGGAA NP_001336851.1:n.81+146_81+149delinsGGAA
NR_146327.2:n.136+146_136+149delinsGGAA