Canonical Allele Identifier: CA2260739023

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999165T= , CM000679.2:g.42999165T=	GRCh38
NC_000017.10:g.41151182T= , CM000679.1:g.41151182T=	GRCh37
NC_000017.9:g.38404708T=	NCBI36
NG_053099.1:g.5893T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+334T= MANE Select	ENSP00000253788.5:n.81+334T=
ENST00000589913.6:c.81+334T=	ENSP00000464813.1:n.81+334T=
ENST00000590864.2:c.82-21T=	ENSP00000467939.2:n.82-21T=
ENST00000253788.9:c.81+334T=	ENSP00000253788.4:n.81+334T=
ENST00000586277.5:c.104+253T=
ENST00000587478.1:n.470T=
ENST00000588830.1:c.81+334T=	ENSP00000468468.1:n.81+334T=
ENST00000589037.5:c.81+334T=	ENSP00000467587.1:n.81+334T=
ENST00000589913.5:c.81+334T=	ENSP00000464813.1:n.81+334T=
ENST00000593262.1:n.747T=
NM_000988.3:c.81+334T=	NP_000979.1:n.81+334T=
NM_000988.5:c.81+334T= MANE Select	NP_000979.1:n.81+334T=
NM_001349921.1:c.81+334T=	NP_001336850.1:n.81+334T=
NM_001349922.1:c.81+334T=	NP_001336851.1:n.81+334T=
NR_146327.1:n.164+334T=
NM_001349921.2:c.81+334T=	NP_001336850.1:n.81+334T=
NM_001349922.2:c.81+334T=	NP_001336851.1:n.81+334T=
NR_146327.2:n.136+334T=