Canonical Allele Identifier: CA656362029

Gene: RPL27

Linked Data

• COSMIC: COSN24378515

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998569dup , CM000679.2:g.42998569dup	GRCh38
NC_000017.10:g.41150586dup , CM000679.1:g.41150586dup	GRCh37
NC_000017.9:g.38404112dup	NCBI36
NG_053099.1:g.5297dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+98dup MANE Select	ENSP00000253788.5:n.-3+98dup
ENST00000589913.6:c.-182dup	ENSP00000464813.1:n.-182dup
ENST00000253788.9:c.-3+98dup	ENSP00000253788.4:n.-3+98dup
ENST00000587478.1:n.53+98dup
ENST00000588830.1:c.-3+98dup	ENSP00000468468.1:n.-3+98dup
ENST00000589037.5:c.-3+154dup	ENSP00000467587.1:n.-3+154dup
ENST00000589913.5:c.-182dup	ENSP00000464813.1:n.-182dup
ENST00000593262.1:n.151dup
NM_000988.3:c.-3+98dup	NP_000979.1:n.-3+98dup
NM_000988.5:c.-3+98dup MANE Select	NP_000979.1:n.-3+98dup
NM_001349921.1:c.-3+154dup	NP_001336850.1:n.-3+154dup
NM_001349922.1:c.-182dup	NP_001336851.1:n.-182dup
NR_146327.1:n.81+98dup
NM_001349921.2:c.-3+154dup	NP_001336850.1:n.-3+154dup
NM_001349922.2:c.-182dup	NP_001336851.1:n.-182dup
NR_146327.2:n.53+98dup