Canonical Allele Identifier: CA2260738741
Gene: RPL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42998639_42998641delinsAAC , CM000679.2:g.42998639_42998641delinsAAC GRCh38
NC_000017.10:g.41150656_41150658delinsAAC , CM000679.1:g.41150656_41150658delinsAAC GRCh37
NC_000017.9:g.38404182_38404184delinsAAC NCBI36
NG_053099.1:g.5367_5369delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.-2-110_-2-108delinsAAC MANE Select ENSP00000253788.5:n.-2-110_-2-108delinsAAC
ENST00000589913.6:c.-112_-110delinsAAC ENSP00000464813.1:n.-112_-110delinsAAC
ENST00000253788.9:c.-2-110_-2-108delinsAAC ENSP00000253788.4:n.-2-110_-2-108delinsAAC
ENST00000587478.1:n.54-110_54-108delinsAAC
ENST00000588830.1:c.-2-110_-2-108delinsAAC ENSP00000468468.1:n.-2-110_-2-108delinsAAC
ENST00000589037.5:c.-2-110_-2-108delinsAAC ENSP00000467587.1:n.-2-110_-2-108delinsAAC
ENST00000589913.5:c.-112_-110delinsAAC ENSP00000464813.1:n.-112_-110delinsAAC
ENST00000593262.1:n.221_223delinsAAC
NM_000988.3:c.-2-110_-2-108delinsAAC NP_000979.1:n.-2-110_-2-108delinsAAC
NM_000988.5:c.-2-110_-2-108delinsAAC MANE Select NP_000979.1:n.-2-110_-2-108delinsAAC
NM_001349921.1:c.-2-110_-2-108delinsAAC NP_001336850.1:n.-2-110_-2-108delinsAAC
NM_001349922.1:c.-112_-110delinsAAC NP_001336851.1:n.-112_-110delinsAAC
NR_146327.1:n.82-110_82-108delinsAAC
NM_001349921.2:c.-2-110_-2-108delinsAAC NP_001336850.1:n.-2-110_-2-108delinsAAC
NM_001349922.2:c.-112_-110delinsAAC NP_001336851.1:n.-112_-110delinsAAC
NR_146327.2:n.54-110_54-108delinsAAC