Canonical Allele Identifier: CA2260739017

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999158_42999165delinsCTTTTCTT , CM000679.2:g.42999158_42999165delinsCTTTTCTT	GRCh38
NC_000017.10:g.41151175_41151182delinsCTTTTCTT , CM000679.1:g.41151175_41151182delinsCTTTTCTT	GRCh37
NC_000017.9:g.38404701_38404708delinsCTTTTCTT	NCBI36
NG_053099.1:g.5886_5893delinsCTTTTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+327_81+334delinsCTTTTCTT MANE Select	ENSP00000253788.5:n.81+327_81+334delinsCTTTTCTT
ENST00000589913.6:c.81+327_81+334delinsCTTTTCTT	ENSP00000464813.1:n.81+327_81+334delinsCTTTTCTT
ENST00000590864.2:c.82-28_82-21delinsCTTTTCTT	ENSP00000467939.2:n.82-28_82-21delinsCTTTTCTT
ENST00000253788.9:c.81+327_81+334delinsCTTTTCTT	ENSP00000253788.4:n.81+327_81+334delinsCTTTTCTT
ENST00000586277.5:c.104+246_104+253delinsCTTTTCTT
ENST00000587478.1:n.463_470delinsCTTTTCTT
ENST00000588830.1:c.81+327_81+334delinsCTTTTCTT	ENSP00000468468.1:n.81+327_81+334delinsCTTTTCTT
ENST00000589037.5:c.81+327_81+334delinsCTTTTCTT	ENSP00000467587.1:n.81+327_81+334delinsCTTTTCTT
ENST00000589913.5:c.81+327_81+334delinsCTTTTCTT	ENSP00000464813.1:n.81+327_81+334delinsCTTTTCTT
ENST00000593262.1:n.740_747delinsCTTTTCTT
NM_000988.3:c.81+327_81+334delinsCTTTTCTT	NP_000979.1:n.81+327_81+334delinsCTTTTCTT
NM_000988.5:c.81+327_81+334delinsCTTTTCTT MANE Select	NP_000979.1:n.81+327_81+334delinsCTTTTCTT
NM_001349921.1:c.81+327_81+334delinsCTTTTCTT	NP_001336850.1:n.81+327_81+334delinsCTTTTCTT
NM_001349922.1:c.81+327_81+334delinsCTTTTCTT	NP_001336851.1:n.81+327_81+334delinsCTTTTCTT
NR_146327.1:n.164+327_164+334delinsCTTTTCTT
NM_001349921.2:c.81+327_81+334delinsCTTTTCTT	NP_001336850.1:n.81+327_81+334delinsCTTTTCTT
NM_001349922.2:c.81+327_81+334delinsCTTTTCTT	NP_001336851.1:n.81+327_81+334delinsCTTTTCTT
NR_146327.2:n.136+327_136+334delinsCTTTTCTT