Canonical Allele Identifier: CA2260738693

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998550T= , CM000679.2:g.42998550T=	GRCh38
NC_000017.10:g.41150567T= , CM000679.1:g.41150567T=	GRCh37
NC_000017.9:g.38404093T=	NCBI36
NG_053099.1:g.5278T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+79T= MANE Select	ENSP00000253788.5:n.-3+79T=
ENST00000589913.6:c.-201T=	ENSP00000464813.1:n.-201T=
ENST00000253788.9:c.-3+79T=	ENSP00000253788.4:n.-3+79T=
ENST00000587478.1:n.53+79T=
ENST00000588830.1:c.-3+79T=	ENSP00000468468.1:n.-3+79T=
ENST00000589037.5:c.-3+135T=	ENSP00000467587.1:n.-3+135T=
ENST00000589913.5:c.-201T=	ENSP00000464813.1:n.-201T=
ENST00000593262.1:n.132T=
NM_000988.3:c.-3+79T=	NP_000979.1:n.-3+79T=
NM_000988.5:c.-3+79T= MANE Select	NP_000979.1:n.-3+79T=
NM_001349921.1:c.-3+135T=	NP_001336850.1:n.-3+135T=
NM_001349922.1:c.-201T=	NP_001336851.1:n.-201T=
NR_146327.1:n.81+79T=
NM_001349921.2:c.-3+135T=	NP_001336850.1:n.-3+135T=
NM_001349922.2:c.-201T=	NP_001336851.1:n.-201T=
NR_146327.2:n.53+79T=