Canonical Allele Identifier: CA2260738800
Gene: RPL27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42998758A= , CM000679.2:g.42998758A= GRCh38
NC_000017.10:g.41150775A= , CM000679.1:g.41150775A= GRCh37
NC_000017.9:g.38404301A= NCBI36
NG_053099.1:g.5486A=

Transcript Alleles

HGVS Amino-acid change
ENST00000253788.12:c.8A= MANE Select ENSP00000253788.5:p.Lys3=
ENST00000589913.6:c.8A= ENSP00000464813.1:p.Lys3=
ENST00000590864.2:c.8A= ENSP00000467939.2:p.Lys3=
ENST00000253788.9:c.8A= ENSP00000253788.4:p.Lys3=
ENST00000587478.1:n.63A=
ENST00000588830.1:c.8A= ENSP00000468468.1:p.Lys3=
ENST00000589037.5:c.8A= ENSP00000467587.1:p.Lys3=
ENST00000589913.5:c.8A= ENSP00000464813.1:p.Lys3=
ENST00000593262.1:n.340A=
NM_000988.3:c.8A= NP_000979.1:p.Lys3=
NM_000988.5:c.8A= MANE Select NP_000979.1:p.Lys3=
NM_001349921.1:c.8A= NP_001336850.1:p.Lys3=
NM_001349922.1:c.8A= NP_001336851.1:p.Lys3=
NR_146327.1:n.91A=
NM_001349921.2:c.8A= NP_001336850.1:p.Lys3=
NM_001349922.2:c.8A= NP_001336851.1:p.Lys3=
NR_146327.2:n.63A=