Canonical Allele Identifier: CA2260738682

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998532G= , CM000679.2:g.42998532G=	GRCh38
NC_000017.10:g.41150549G= , CM000679.1:g.41150549G=	GRCh37
NC_000017.9:g.38404075G=	NCBI36
NG_053099.1:g.5260G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+61G= MANE Select	ENSP00000253788.5:n.-3+61G=
ENST00000589913.6:c.-219G=	ENSP00000464813.1:n.-219G=
ENST00000253788.9:c.-3+61G=	ENSP00000253788.4:n.-3+61G=
ENST00000587478.1:n.53+61G=
ENST00000588830.1:c.-3+61G=	ENSP00000468468.1:n.-3+61G=
ENST00000589037.5:c.-3+117G=	ENSP00000467587.1:n.-3+117G=
ENST00000589913.5:c.-219G=	ENSP00000464813.1:n.-219G=
ENST00000593262.1:n.114G=
NM_000988.3:c.-3+61G=	NP_000979.1:n.-3+61G=
NM_000988.5:c.-3+61G= MANE Select	NP_000979.1:n.-3+61G=
NM_001349921.1:c.-3+117G=	NP_001336850.1:n.-3+117G=
NM_001349922.1:c.-219G=	NP_001336851.1:n.-219G=
NR_146327.1:n.81+61G=
NM_001349921.2:c.-3+117G=	NP_001336850.1:n.-3+117G=
NM_001349922.2:c.-219G=	NP_001336851.1:n.-219G=
NR_146327.2:n.53+61G=