Canonical Allele Identifier: CA2638053359
Gene: RPL27 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42998564A>C , CM000679.2:g.42998564A>C GRCh38
NC_000017.10:g.41150581A>C , CM000679.1:g.41150581A>C GRCh37
NC_000017.9:g.38404107A>C NCBI36
NG_053099.1:g.5292A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253788.12:c.-3+93A>C MANE Select ENSP00000253788.5:n.-3+93A>C
ENST00000589913.6:c.-187A>C ENSP00000464813.1:n.-187A>C
ENST00000253788.9:c.-3+93A>C ENSP00000253788.4:n.-3+93A>C
ENST00000587478.1:n.53+93A>C
ENST00000588830.1:c.-3+93A>C ENSP00000468468.1:n.-3+93A>C
ENST00000589037.5:c.-3+149A>C ENSP00000467587.1:n.-3+149A>C
ENST00000589913.5:c.-187A>C ENSP00000464813.1:n.-187A>C
ENST00000593262.1:n.146A>C
NM_000988.3:c.-3+93A>C NP_000979.1:n.-3+93A>C
NM_000988.5:c.-3+93A>C MANE Select NP_000979.1:n.-3+93A>C
NM_001349921.1:c.-3+149A>C NP_001336850.1:n.-3+149A>C
NM_001349922.1:c.-187A>C NP_001336851.1:n.-187A>C
NR_146327.1:n.81+93A>C
NM_001349921.2:c.-3+149A>C NP_001336850.1:n.-3+149A>C
NM_001349922.2:c.-187A>C NP_001336851.1:n.-187A>C
NR_146327.2:n.53+93A>C