Canonical Allele Identifier: CA2638053590
Gene: RPL27 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42998671G>T , CM000679.2:g.42998671G>T GRCh38
NC_000017.10:g.41150688G>T , CM000679.1:g.41150688G>T GRCh37
NC_000017.9:g.38404214G>T NCBI36
NG_053099.1:g.5399G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000253788.12:c.-2-78G>T MANE Select ENSP00000253788.5:n.-2-78G>T
ENST00000589913.6:c.-80G>T ENSP00000464813.1:n.-80G>T
ENST00000253788.9:c.-2-78G>T ENSP00000253788.4:n.-2-78G>T
ENST00000587478.1:n.54-78G>T
ENST00000588830.1:c.-2-78G>T ENSP00000468468.1:n.-2-78G>T
ENST00000589037.5:c.-2-78G>T ENSP00000467587.1:n.-2-78G>T
ENST00000589913.5:c.-80G>T ENSP00000464813.1:n.-80G>T
ENST00000593262.1:n.253G>T
NM_000988.3:c.-2-78G>T NP_000979.1:n.-2-78G>T
NM_000988.5:c.-2-78G>T MANE Select NP_000979.1:n.-2-78G>T
NM_001349921.1:c.-2-78G>T NP_001336850.1:n.-2-78G>T
NM_001349922.1:c.-80G>T NP_001336851.1:n.-80G>T
NR_146327.1:n.82-78G>T
NM_001349921.2:c.-2-78G>T NP_001336850.1:n.-2-78G>T
NM_001349922.2:c.-80G>T NP_001336851.1:n.-80G>T
NR_146327.2:n.54-78G>T