Canonical Allele Identifier: CA2260738709

Gene: RPL27

Linked Data

• dbSNP Id: rs2050324493

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998577C>G , CM000679.2:g.42998577C>G	GRCh38
NC_000017.10:g.41150594C>G , CM000679.1:g.41150594C>G	GRCh37
NC_000017.9:g.38404120C>G	NCBI36
NG_053099.1:g.5305C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+106C>G MANE Select	ENSP00000253788.5:n.-3+106C>G
ENST00000589913.6:c.-174C>G	ENSP00000464813.1:n.-174C>G
ENST00000253788.9:c.-3+106C>G	ENSP00000253788.4:n.-3+106C>G
ENST00000587478.1:n.53+106C>G
ENST00000588830.1:c.-3+106C>G	ENSP00000468468.1:n.-3+106C>G
ENST00000589037.5:c.-3+162C>G	ENSP00000467587.1:n.-3+162C>G
ENST00000589913.5:c.-174C>G	ENSP00000464813.1:n.-174C>G
ENST00000593262.1:n.159C>G
NM_000988.3:c.-3+106C>G	NP_000979.1:n.-3+106C>G
NM_000988.5:c.-3+106C>G MANE Select	NP_000979.1:n.-3+106C>G
NM_001349921.1:c.-3+162C>G	NP_001336850.1:n.-3+162C>G
NM_001349922.1:c.-174C>G	NP_001336851.1:n.-174C>G
NR_146327.1:n.81+106C>G
NM_001349921.2:c.-3+162C>G	NP_001336850.1:n.-3+162C>G
NM_001349922.2:c.-174C>G	NP_001336851.1:n.-174C>G
NR_146327.2:n.53+106C>G