Canonical Allele Identifier: CA2260739013

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999152_42999157delinsCCTTTT , CM000679.2:g.42999152_42999157delinsCCTTTT	GRCh38
NC_000017.10:g.41151169_41151174delinsCCTTTT , CM000679.1:g.41151169_41151174delinsCCTTTT	GRCh37
NC_000017.9:g.38404695_38404700delinsCCTTTT	NCBI36
NG_053099.1:g.5880_5885delinsCCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+321_81+326delinsCCTTTT MANE Select	ENSP00000253788.5:n.81+321_81+326delinsCCTTTT
ENST00000589913.6:c.81+321_81+326delinsCCTTTT	ENSP00000464813.1:n.81+321_81+326delinsCCTTTT
ENST00000590864.2:c.82-34_82-29delinsCCTTTT	ENSP00000467939.2:n.82-34_82-29delinsCCTTTT
ENST00000253788.9:c.81+321_81+326delinsCCTTTT	ENSP00000253788.4:n.81+321_81+326delinsCCTTTT
ENST00000586277.5:c.104+240_104+245delinsCCTTTT
ENST00000587478.1:n.457_462delinsCCTTTT
ENST00000588830.1:c.81+321_81+326delinsCCTTTT	ENSP00000468468.1:n.81+321_81+326delinsCCTTTT
ENST00000589037.5:c.81+321_81+326delinsCCTTTT	ENSP00000467587.1:n.81+321_81+326delinsCCTTTT
ENST00000589913.5:c.81+321_81+326delinsCCTTTT	ENSP00000464813.1:n.81+321_81+326delinsCCTTTT
ENST00000593262.1:n.734_739delinsCCTTTT
NM_000988.3:c.81+321_81+326delinsCCTTTT	NP_000979.1:n.81+321_81+326delinsCCTTTT
NM_000988.5:c.81+321_81+326delinsCCTTTT MANE Select	NP_000979.1:n.81+321_81+326delinsCCTTTT
NM_001349921.1:c.81+321_81+326delinsCCTTTT	NP_001336850.1:n.81+321_81+326delinsCCTTTT
NM_001349922.1:c.81+321_81+326delinsCCTTTT	NP_001336851.1:n.81+321_81+326delinsCCTTTT
NR_146327.1:n.164+321_164+326delinsCCTTTT
NM_001349921.2:c.81+321_81+326delinsCCTTTT	NP_001336850.1:n.81+321_81+326delinsCCTTTT
NM_001349922.2:c.81+321_81+326delinsCCTTTT	NP_001336851.1:n.81+321_81+326delinsCCTTTT
NR_146327.2:n.136+321_136+326delinsCCTTTT