Canonical Allele Identifier: CA2260738831

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998844C= , CM000679.2:g.42998844C=	GRCh38
NC_000017.10:g.41150861C= , CM000679.1:g.41150861C=	GRCh37
NC_000017.9:g.38404387C=	NCBI36
NG_053099.1:g.5572C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+13C= MANE Select	ENSP00000253788.5:n.81+13C=
ENST00000589913.6:c.81+13C=	ENSP00000464813.1:n.81+13C=
ENST00000590864.2:c.81+13C=	ENSP00000467939.2:n.81+13C=
ENST00000253788.9:c.81+13C=	ENSP00000253788.4:n.81+13C=
ENST00000586277.5:c.36C=
ENST00000587478.1:n.149C=
ENST00000588830.1:c.81+13C=	ENSP00000468468.1:n.81+13C=
ENST00000589037.5:c.81+13C=	ENSP00000467587.1:n.81+13C=
ENST00000589913.5:c.81+13C=	ENSP00000464813.1:n.81+13C=
ENST00000593262.1:n.426C=
NM_000988.3:c.81+13C=	NP_000979.1:n.81+13C=
NM_000988.5:c.81+13C= MANE Select	NP_000979.1:n.81+13C=
NM_001349921.1:c.81+13C=	NP_001336850.1:n.81+13C=
NM_001349922.1:c.81+13C=	NP_001336851.1:n.81+13C=
NR_146327.1:n.164+13C=
NM_001349921.2:c.81+13C=	NP_001336850.1:n.81+13C=
NM_001349922.2:c.81+13C=	NP_001336851.1:n.81+13C=
NR_146327.2:n.136+13C=