Canonical Allele Identifier: CA2260739030

Gene: RPL27

Linked Data

• dbSNP Id: rs2050332608
• gnomAD v4: 17-42999171-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999172_42999173insCT , CM000679.2:g.42999172_42999173insCT	GRCh38
NC_000017.10:g.41151189_41151190insCT , CM000679.1:g.41151189_41151190insCT	GRCh37
NC_000017.9:g.38404715_38404716insCT	NCBI36
NG_053099.1:g.5900_5901insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+341_81+342insCT MANE Select	ENSP00000253788.5:n.81+341_81+342insCT
ENST00000589913.6:c.81+341_81+342insCT	ENSP00000464813.1:n.81+341_81+342insCT
ENST00000590864.2:c.82-14_82-13insCT	ENSP00000467939.2:n.82-14_82-13insCT
ENST00000253788.9:c.81+341_81+342insCT	ENSP00000253788.4:n.81+341_81+342insCT
ENST00000586277.5:c.104+260_104+261insCT
ENST00000587478.1:n.477_478insCT
ENST00000588830.1:c.81+341_81+342insCT	ENSP00000468468.1:n.81+341_81+342insCT
ENST00000589037.5:c.81+341_81+342insCT	ENSP00000467587.1:n.81+341_81+342insCT
ENST00000589913.5:c.81+341_81+342insCT	ENSP00000464813.1:n.81+341_81+342insCT
ENST00000593262.1:n.754_755insCT
NM_000988.3:c.81+341_81+342insCT	NP_000979.1:n.81+341_81+342insCT
NM_000988.5:c.81+341_81+342insCT MANE Select	NP_000979.1:n.81+341_81+342insCT
NM_001349921.1:c.81+341_81+342insCT	NP_001336850.1:n.81+341_81+342insCT
NM_001349922.1:c.81+341_81+342insCT	NP_001336851.1:n.81+341_81+342insCT
NR_146327.1:n.164+341_164+342insCT
NM_001349921.2:c.81+341_81+342insCT	NP_001336850.1:n.81+341_81+342insCT
NM_001349922.2:c.81+341_81+342insCT	NP_001336851.1:n.81+341_81+342insCT
NR_146327.2:n.136+341_136+342insCT