Canonical Allele Identifier: CA2638054660

Gene: RPL27

Linked Data

• gnomAD v4: 17-42999167-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999167_42999168insA , CM000679.2:g.42999167_42999168insA	GRCh38
NC_000017.10:g.41151184_41151185insA , CM000679.1:g.41151184_41151185insA	GRCh37
NC_000017.9:g.38404710_38404711insA	NCBI36
NG_053099.1:g.5895_5896insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+336_81+337insA MANE Select	ENSP00000253788.5:n.81+336_81+337insA
ENST00000589913.6:c.81+336_81+337insA	ENSP00000464813.1:n.81+336_81+337insA
ENST00000590864.2:c.82-19_82-18insA	ENSP00000467939.2:n.82-19_82-18insA
ENST00000253788.9:c.81+336_81+337insA	ENSP00000253788.4:n.81+336_81+337insA
ENST00000586277.5:c.104+255_104+256insA
ENST00000587478.1:n.472_473insA
ENST00000588830.1:c.81+336_81+337insA	ENSP00000468468.1:n.81+336_81+337insA
ENST00000589037.5:c.81+336_81+337insA	ENSP00000467587.1:n.81+336_81+337insA
ENST00000589913.5:c.81+336_81+337insA	ENSP00000464813.1:n.81+336_81+337insA
ENST00000593262.1:n.749_750insA
NM_000988.3:c.81+336_81+337insA	NP_000979.1:n.81+336_81+337insA
NM_000988.5:c.81+336_81+337insA MANE Select	NP_000979.1:n.81+336_81+337insA
NM_001349921.1:c.81+336_81+337insA	NP_001336850.1:n.81+336_81+337insA
NM_001349922.1:c.81+336_81+337insA	NP_001336851.1:n.81+336_81+337insA
NR_146327.1:n.164+336_164+337insA
NM_001349921.2:c.81+336_81+337insA	NP_001336850.1:n.81+336_81+337insA
NM_001349922.2:c.81+336_81+337insA	NP_001336851.1:n.81+336_81+337insA
NR_146327.2:n.136+336_136+337insA