Canonical Allele Identifier: CA2594127961

Gene: RPL27

Linked Data

• dbSNP Id: rs2151964686
• gnomAD v3: 17-42999114-ATT-A
• gnomAD v4: 17-42999114-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999115_42999116del , CM000679.2:g.42999115_42999116del	GRCh38
NC_000017.10:g.41151132_41151133del , CM000679.1:g.41151132_41151133del	GRCh37
NC_000017.9:g.38404658_38404659del	NCBI36
NG_053099.1:g.5843_5844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+284_81+285del MANE Select	ENSP00000253788.5:n.81+284_81+285del
ENST00000589913.6:c.81+284_81+285del	ENSP00000464813.1:n.81+284_81+285del
ENST00000590864.2:c.82-71_82-70del	ENSP00000467939.2:n.82-71_82-70del
ENST00000253788.9:c.81+284_81+285del	ENSP00000253788.4:n.81+284_81+285del
ENST00000586277.5:c.104+203_104+204del
ENST00000587478.1:n.420_421del
ENST00000588830.1:c.81+284_81+285del	ENSP00000468468.1:n.81+284_81+285del
ENST00000589037.5:c.81+284_81+285del	ENSP00000467587.1:n.81+284_81+285del
ENST00000589913.5:c.81+284_81+285del	ENSP00000464813.1:n.81+284_81+285del
ENST00000593262.1:n.697_698del
NM_000988.3:c.81+284_81+285del	NP_000979.1:n.81+284_81+285del
NM_000988.5:c.81+284_81+285del MANE Select	NP_000979.1:n.81+284_81+285del
NM_001349921.1:c.81+284_81+285del	NP_001336850.1:n.81+284_81+285del
NM_001349922.1:c.81+284_81+285del	NP_001336851.1:n.81+284_81+285del
NR_146327.1:n.164+284_164+285del
NM_001349921.2:c.81+284_81+285del	NP_001336850.1:n.81+284_81+285del
NM_001349922.2:c.81+284_81+285del	NP_001336851.1:n.81+284_81+285del
NR_146327.2:n.136+284_136+285del