Canonical Allele Identifier: CA2260738919

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998977G= , CM000679.2:g.42998977G=	GRCh38
NC_000017.10:g.41150994G= , CM000679.1:g.41150994G=	GRCh37
NC_000017.9:g.38404520G=	NCBI36
NG_053099.1:g.5705G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+146G= MANE Select	ENSP00000253788.5:n.81+146G=
ENST00000589913.6:c.81+146G=	ENSP00000464813.1:n.81+146G=
ENST00000590864.2:c.81+146G=	ENSP00000467939.2:n.81+146G=
ENST00000253788.9:c.81+146G=	ENSP00000253788.4:n.81+146G=
ENST00000586277.5:c.104+65G=
ENST00000587478.1:n.282G=
ENST00000588830.1:c.81+146G=	ENSP00000468468.1:n.81+146G=
ENST00000589037.5:c.81+146G=	ENSP00000467587.1:n.81+146G=
ENST00000589913.5:c.81+146G=	ENSP00000464813.1:n.81+146G=
ENST00000593262.1:n.559G=
NM_000988.3:c.81+146G=	NP_000979.1:n.81+146G=
NM_000988.5:c.81+146G= MANE Select	NP_000979.1:n.81+146G=
NM_001349921.1:c.81+146G=	NP_001336850.1:n.81+146G=
NM_001349922.1:c.81+146G=	NP_001336851.1:n.81+146G=
NR_146327.1:n.164+146G=
NM_001349921.2:c.81+146G=	NP_001336850.1:n.81+146G=
NM_001349922.2:c.81+146G=	NP_001336851.1:n.81+146G=
NR_146327.2:n.136+146G=