Canonical Allele Identifier: CA2260738728
Gene: RPL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42998612_42998613delinsCG , CM000679.2:g.42998612_42998613delinsCG GRCh38
NC_000017.10:g.41150629_41150630delinsCG , CM000679.1:g.41150629_41150630delinsCG GRCh37
NC_000017.9:g.38404155_38404156delinsCG NCBI36
NG_053099.1:g.5340_5341delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.-2-137_-2-136delinsCG MANE Select ENSP00000253788.5:n.-2-137_-2-136delinsCG
ENST00000589913.6:c.-139_-138delinsCG ENSP00000464813.1:n.-139_-138delinsCG
ENST00000253788.9:c.-2-137_-2-136delinsCG ENSP00000253788.4:n.-2-137_-2-136delinsCG
ENST00000587478.1:n.54-137_54-136delinsCG
ENST00000588830.1:c.-2-137_-2-136delinsCG ENSP00000468468.1:n.-2-137_-2-136delinsCG
ENST00000589037.5:c.-2-137_-2-136delinsCG ENSP00000467587.1:n.-2-137_-2-136delinsCG
ENST00000589913.5:c.-139_-138delinsCG ENSP00000464813.1:n.-139_-138delinsCG
ENST00000593262.1:n.194_195delinsCG
NM_000988.3:c.-2-137_-2-136delinsCG NP_000979.1:n.-2-137_-2-136delinsCG
NM_000988.5:c.-2-137_-2-136delinsCG MANE Select NP_000979.1:n.-2-137_-2-136delinsCG
NM_001349921.1:c.-2-137_-2-136delinsCG NP_001336850.1:n.-2-137_-2-136delinsCG
NM_001349922.1:c.-139_-138delinsCG NP_001336851.1:n.-139_-138delinsCG
NR_146327.1:n.82-137_82-136delinsCG
NM_001349921.2:c.-2-137_-2-136delinsCG NP_001336850.1:n.-2-137_-2-136delinsCG
NM_001349922.2:c.-139_-138delinsCG NP_001336851.1:n.-139_-138delinsCG
NR_146327.2:n.54-137_54-136delinsCG