Canonical Allele Identifier: CA2260738630

Gene: RPL27

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998458G= , CM000679.2:g.42998458G=	GRCh38
NC_000017.10:g.41150475G= , CM000679.1:g.41150475G=	GRCh37
NC_000017.9:g.38404001G=	NCBI36
NG_053099.1:g.5186G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-16G= MANE Select	ENSP00000253788.5:n.-16G=
ENST00000253788.9:c.-16G=	ENSP00000253788.4:n.-16G=
ENST00000587478.1:n.40G=
ENST00000588830.1:c.-16G=	ENSP00000468468.1:n.-16G=
ENST00000589037.5:c.-3+43G=	ENSP00000467587.1:n.-3+43G=
ENST00000593262.1:n.40G=
NM_000988.3:c.-16G=	NP_000979.1:n.-16G=
NM_000988.5:c.-16G= MANE Select	NP_000979.1:n.-16G=
NM_001349921.1:c.-3+43G=	NP_001336850.1:n.-3+43G=
NR_146327.1:n.68G=
NM_001349921.2:c.-3+43G=	NP_001336850.1:n.-3+43G=
NM_001349922.2:c.-293G=	NP_001336851.1:n.-293G=
NR_146327.2:n.40G=