Canonical Allele Identifier: CA2260738960

Gene: RPL27

Linked Data

• dbSNP Id: rs2050331132

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999035_42999037del , CM000679.2:g.42999035_42999037del	GRCh38
NC_000017.10:g.41151052_41151054del , CM000679.1:g.41151052_41151054del	GRCh37
NC_000017.9:g.38404578_38404580del	NCBI36
NG_053099.1:g.5763_5765del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+204_81+206del MANE Select	ENSP00000253788.5:n.81+204_81+206del
ENST00000589913.6:c.81+204_81+206del	ENSP00000464813.1:n.81+204_81+206del
ENST00000590864.2:c.82-151_82-149del	ENSP00000467939.2:n.82-151_82-149del
ENST00000253788.9:c.81+204_81+206del	ENSP00000253788.4:n.81+204_81+206del
ENST00000586277.5:c.104+123_104+125del
ENST00000587478.1:n.340_342del
ENST00000588830.1:c.81+204_81+206del	ENSP00000468468.1:n.81+204_81+206del
ENST00000589037.5:c.81+204_81+206del	ENSP00000467587.1:n.81+204_81+206del
ENST00000589913.5:c.81+204_81+206del	ENSP00000464813.1:n.81+204_81+206del
ENST00000593262.1:n.617_619del
NM_000988.3:c.81+204_81+206del	NP_000979.1:n.81+204_81+206del
NM_000988.5:c.81+204_81+206del MANE Select	NP_000979.1:n.81+204_81+206del
NM_001349921.1:c.81+204_81+206del	NP_001336850.1:n.81+204_81+206del
NM_001349922.1:c.81+204_81+206del	NP_001336851.1:n.81+204_81+206del
NR_146327.1:n.164+204_164+206del
NM_001349921.2:c.81+204_81+206del	NP_001336850.1:n.81+204_81+206del
NM_001349922.2:c.81+204_81+206del	NP_001336851.1:n.81+204_81+206del
NR_146327.2:n.136+204_136+206del