Canonical Allele Identifier: CA2260738821

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998823A= , CM000679.2:g.42998823A=	GRCh38
NC_000017.10:g.41150840A= , CM000679.1:g.41150840A=	GRCh37
NC_000017.9:g.38404366A=	NCBI36
NG_053099.1:g.5551A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.73A= MANE Select	ENSP00000253788.5:p.Ile25=
ENST00000589913.6:c.73A=	ENSP00000464813.1:p.Ile25=
ENST00000590864.2:c.73A=	ENSP00000467939.2:p.Ile25=
ENST00000253788.9:c.73A=	ENSP00000253788.4:p.Ile25=
ENST00000586277.5:c.15A=
ENST00000587478.1:n.128A=
ENST00000588830.1:c.73A=	ENSP00000468468.1:p.Ile25=
ENST00000589037.5:c.73A=	ENSP00000467587.1:p.Ile25=
ENST00000589913.5:c.73A=	ENSP00000464813.1:p.Ile25=
ENST00000593262.1:n.405A=
NM_000988.3:c.73A=	NP_000979.1:p.Ile25=
NM_000988.5:c.73A= MANE Select	NP_000979.1:p.Ile25=
NM_001349921.1:c.73A=	NP_001336850.1:p.Ile25=
NM_001349922.1:c.73A=	NP_001336851.1:p.Ile25=
NR_146327.1:n.156A=
NM_001349921.2:c.73A=	NP_001336850.1:p.Ile25=
NM_001349922.2:c.73A=	NP_001336851.1:p.Ile25=
NR_146327.2:n.128A=