Canonical Allele Identifier: CA2638054629

Gene: RPL27

Linked Data

• gnomAD v4: 17-42999158-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999161_42999162del , CM000679.2:g.42999161_42999162del	GRCh38
NC_000017.10:g.41151178_41151179del , CM000679.1:g.41151178_41151179del	GRCh37
NC_000017.9:g.38404704_38404705del	NCBI36
NG_053099.1:g.5889_5890del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+330_81+331del MANE Select	ENSP00000253788.5:n.81+330_81+331del
ENST00000589913.6:c.81+330_81+331del	ENSP00000464813.1:n.81+330_81+331del
ENST00000590864.2:c.82-25_82-24del	ENSP00000467939.2:n.82-25_82-24del
ENST00000253788.9:c.81+330_81+331del	ENSP00000253788.4:n.81+330_81+331del
ENST00000586277.5:c.104+249_104+250del
ENST00000587478.1:n.466_467del
ENST00000588830.1:c.81+330_81+331del	ENSP00000468468.1:n.81+330_81+331del
ENST00000589037.5:c.81+330_81+331del	ENSP00000467587.1:n.81+330_81+331del
ENST00000589913.5:c.81+330_81+331del	ENSP00000464813.1:n.81+330_81+331del
ENST00000593262.1:n.743_744del
NM_000988.3:c.81+330_81+331del	NP_000979.1:n.81+330_81+331del
NM_000988.5:c.81+330_81+331del MANE Select	NP_000979.1:n.81+330_81+331del
NM_001349921.1:c.81+330_81+331del	NP_001336850.1:n.81+330_81+331del
NM_001349922.1:c.81+330_81+331del	NP_001336851.1:n.81+330_81+331del
NR_146327.1:n.164+330_164+331del
NM_001349921.2:c.81+330_81+331del	NP_001336850.1:n.81+330_81+331del
NM_001349922.2:c.81+330_81+331del	NP_001336851.1:n.81+330_81+331del
NR_146327.2:n.136+330_136+331del