Canonical Allele Identifier: CA2260738641

Gene: RPL27

Linked Data

• dbSNP Id: rs2050322969

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998468dup , CM000679.2:g.42998468dup	GRCh38
NC_000017.10:g.41150485dup , CM000679.1:g.41150485dup	GRCh37
NC_000017.9:g.38404011dup	NCBI36
NG_053099.1:g.5196dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-6dup MANE Select	ENSP00000253788.5:n.-6dup
ENST00000253788.9:c.-6dup	ENSP00000253788.4:n.-6dup
ENST00000587478.1:n.50dup
ENST00000588830.1:c.-6dup	ENSP00000468468.1:n.-6dup
ENST00000589037.5:c.-3+53dup	ENSP00000467587.1:n.-3+53dup
ENST00000593262.1:n.50dup
NM_000988.3:c.-6dup	NP_000979.1:n.-6dup
NM_000988.5:c.-6dup MANE Select	NP_000979.1:n.-6dup
NM_001349921.1:c.-3+53dup	NP_001336850.1:n.-3+53dup
NM_001349922.1:c.-283dup	NP_001336851.1:n.-283dup
NR_146327.1:n.78dup
NM_001349921.2:c.-3+53dup	NP_001336850.1:n.-3+53dup
NM_001349922.2:c.-283dup	NP_001336851.1:n.-283dup
NR_146327.2:n.50dup