Canonical Allele Identifier: CA2260739016

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999153_42999154delinsCT , CM000679.2:g.42999153_42999154delinsCT	GRCh38
NC_000017.10:g.41151170_41151171delinsCT , CM000679.1:g.41151170_41151171delinsCT	GRCh37
NC_000017.9:g.38404696_38404697delinsCT	NCBI36
NG_053099.1:g.5881_5882delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+322_81+323delinsCT MANE Select	ENSP00000253788.5:n.81+322_81+323delinsCT
ENST00000589913.6:c.81+322_81+323delinsCT	ENSP00000464813.1:n.81+322_81+323delinsCT
ENST00000590864.2:c.82-33_82-32delinsCT	ENSP00000467939.2:n.82-33_82-32delinsCT
ENST00000253788.9:c.81+322_81+323delinsCT	ENSP00000253788.4:n.81+322_81+323delinsCT
ENST00000586277.5:c.104+241_104+242delinsCT
ENST00000587478.1:n.458_459delinsCT
ENST00000588830.1:c.81+322_81+323delinsCT	ENSP00000468468.1:n.81+322_81+323delinsCT
ENST00000589037.5:c.81+322_81+323delinsCT	ENSP00000467587.1:n.81+322_81+323delinsCT
ENST00000589913.5:c.81+322_81+323delinsCT	ENSP00000464813.1:n.81+322_81+323delinsCT
ENST00000593262.1:n.735_736delinsCT
NM_000988.3:c.81+322_81+323delinsCT	NP_000979.1:n.81+322_81+323delinsCT
NM_000988.5:c.81+322_81+323delinsCT MANE Select	NP_000979.1:n.81+322_81+323delinsCT
NM_001349921.1:c.81+322_81+323delinsCT	NP_001336850.1:n.81+322_81+323delinsCT
NM_001349922.1:c.81+322_81+323delinsCT	NP_001336851.1:n.81+322_81+323delinsCT
NR_146327.1:n.164+322_164+323delinsCT
NM_001349921.2:c.81+322_81+323delinsCT	NP_001336850.1:n.81+322_81+323delinsCT
NM_001349922.2:c.81+322_81+323delinsCT	NP_001336851.1:n.81+322_81+323delinsCT
NR_146327.2:n.136+322_136+323delinsCT