Canonical Allele Identifier: CA2260738818

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998812G= , CM000679.2:g.42998812G=	GRCh38
NC_000017.10:g.41150829G= , CM000679.1:g.41150829G=	GRCh37
NC_000017.9:g.38404355G=	NCBI36
NG_053099.1:g.5540G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.62G= MANE Select	ENSP00000253788.5:p.Arg21=
ENST00000589913.6:c.62G=	ENSP00000464813.1:p.Arg21=
ENST00000590864.2:c.62G=	ENSP00000467939.2:p.Arg21=
ENST00000253788.9:c.62G=	ENSP00000253788.4:p.Arg21=
ENST00000586277.5:c.4G=
ENST00000587478.1:n.117G=
ENST00000588830.1:c.62G=	ENSP00000468468.1:p.Arg21=
ENST00000589037.5:c.62G=	ENSP00000467587.1:p.Arg21=
ENST00000589913.5:c.62G=	ENSP00000464813.1:p.Arg21=
ENST00000593262.1:n.394G=
NM_000988.3:c.62G=	NP_000979.1:p.Arg21=
NM_000988.5:c.62G= MANE Select	NP_000979.1:p.Arg21=
NM_001349921.1:c.62G=	NP_001336850.1:p.Arg21=
NM_001349922.1:c.62G=	NP_001336851.1:p.Arg21=
NR_146327.1:n.145G=
NM_001349921.2:c.62G=	NP_001336850.1:p.Arg21=
NM_001349922.2:c.62G=	NP_001336851.1:p.Arg21=
NR_146327.2:n.117G=