Canonical Allele Identifier: CA2260738710

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998581G= , CM000679.2:g.42998581G=	GRCh38
NC_000017.10:g.41150598G= , CM000679.1:g.41150598G=	GRCh37
NC_000017.9:g.38404124G=	NCBI36
NG_053099.1:g.5309G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+110G= MANE Select	ENSP00000253788.5:n.-3+110G=
ENST00000589913.6:c.-170G=	ENSP00000464813.1:n.-170G=
ENST00000253788.9:c.-3+110G=	ENSP00000253788.4:n.-3+110G=
ENST00000587478.1:n.53+110G=
ENST00000588830.1:c.-3+110G=	ENSP00000468468.1:n.-3+110G=
ENST00000589037.5:c.-3+166G=	ENSP00000467587.1:n.-3+166G=
ENST00000589913.5:c.-170G=	ENSP00000464813.1:n.-170G=
ENST00000593262.1:n.163G=
NM_000988.3:c.-3+110G=	NP_000979.1:n.-3+110G=
NM_000988.5:c.-3+110G= MANE Select	NP_000979.1:n.-3+110G=
NM_001349921.1:c.-3+166G=	NP_001336850.1:n.-3+166G=
NM_001349922.1:c.-170G=	NP_001336851.1:n.-170G=
NR_146327.1:n.81+110G=
NM_001349921.2:c.-3+166G=	NP_001336850.1:n.-3+166G=
NM_001349922.2:c.-170G=	NP_001336851.1:n.-170G=
NR_146327.2:n.53+110G=