Canonical Allele Identifier: CA2547371621

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999164_42999165insAT , CM000679.2:g.42999164_42999165insAT	GRCh38
NC_000017.10:g.41151181_41151182insAT , CM000679.1:g.41151181_41151182insAT	GRCh37
NC_000017.9:g.38404707_38404708insAT	NCBI36
NG_053099.1:g.5892_5893insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+333_81+334insAT MANE Select	ENSP00000253788.5:n.81+333_81+334insAT
ENST00000589913.6:c.81+333_81+334insAT	ENSP00000464813.1:n.81+333_81+334insAT
ENST00000590864.2:c.82-22_82-21insAT	ENSP00000467939.2:n.82-22_82-21insAT
ENST00000253788.9:c.81+333_81+334insAT	ENSP00000253788.4:n.81+333_81+334insAT
ENST00000586277.5:c.104+252_104+253insAT
ENST00000587478.1:n.469_470insAT
ENST00000588830.1:c.81+333_81+334insAT	ENSP00000468468.1:n.81+333_81+334insAT
ENST00000589037.5:c.81+333_81+334insAT	ENSP00000467587.1:n.81+333_81+334insAT
ENST00000589913.5:c.81+333_81+334insAT	ENSP00000464813.1:n.81+333_81+334insAT
ENST00000593262.1:n.746_747insAT
NM_000988.3:c.81+333_81+334insAT	NP_000979.1:n.81+333_81+334insAT
NM_000988.5:c.81+333_81+334insAT MANE Select	NP_000979.1:n.81+333_81+334insAT
NM_001349921.1:c.81+333_81+334insAT	NP_001336850.1:n.81+333_81+334insAT
NM_001349922.1:c.81+333_81+334insAT	NP_001336851.1:n.81+333_81+334insAT
NR_146327.1:n.164+333_164+334insAT
NM_001349921.2:c.81+333_81+334insAT	NP_001336850.1:n.81+333_81+334insAT
NM_001349922.2:c.81+333_81+334insAT	NP_001336851.1:n.81+333_81+334insAT
NR_146327.2:n.136+333_136+334insAT