Canonical Allele Identifier: CA399675719
Gene: RPL27 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.8A>C MANE Select ENSP00000253788.5:p.Lys3Thr
ENST00000589913.6:c.8A>C ENSP00000464813.1:p.Lys3Thr
ENST00000590864.2:c.8A>C ENSP00000467939.2:p.Lys3Thr
ENST00000253788.9:c.8A>C ENSP00000253788.4:p.Lys3Thr
ENST00000587478.1:n.63A>C
ENST00000588830.1:c.8A>C ENSP00000468468.1:p.Lys3Thr
ENST00000589037.5:c.8A>C ENSP00000467587.1:p.Lys3Thr
ENST00000589913.5:c.8A>C ENSP00000464813.1:p.Lys3Thr
ENST00000593262.1:n.340A>C
NM_000988.3:c.8A>C NP_000979.1:p.Lys3Thr
NM_000988.5:c.8A>C MANE Select NP_000979.1:p.Lys3Thr
NM_001349921.1:c.8A>C NP_001336850.1:p.Lys3Thr
NM_001349922.1:c.8A>C NP_001336851.1:p.Lys3Thr
NR_146327.1:n.91A>C
NM_001349921.2:c.8A>C NP_001336850.1:p.Lys3Thr
NM_001349922.2:c.8A>C NP_001336851.1:p.Lys3Thr
NR_146327.2:n.63A>C