Canonical Allele Identifier: CA2638053454

Gene: RPL27

Linked Data

• gnomAD v4: 17-42998598-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998598G>A , CM000679.2:g.42998598G>A	GRCh38
NC_000017.10:g.41150615G>A , CM000679.1:g.41150615G>A	GRCh37
NC_000017.9:g.38404141G>A	NCBI36
NG_053099.1:g.5326G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+127G>A MANE Select	ENSP00000253788.5:n.-3+127G>A
ENST00000589913.6:c.-153G>A	ENSP00000464813.1:n.-153G>A
ENST00000253788.9:c.-3+127G>A	ENSP00000253788.4:n.-3+127G>A
ENST00000587478.1:n.53+127G>A
ENST00000588830.1:c.-3+127G>A	ENSP00000468468.1:n.-3+127G>A
ENST00000589037.5:c.-2-151G>A	ENSP00000467587.1:n.-2-151G>A
ENST00000589913.5:c.-153G>A	ENSP00000464813.1:n.-153G>A
ENST00000593262.1:n.180G>A
NM_000988.3:c.-3+127G>A	NP_000979.1:n.-3+127G>A
NM_000988.5:c.-3+127G>A MANE Select	NP_000979.1:n.-3+127G>A
NM_001349921.1:c.-2-151G>A	NP_001336850.1:n.-2-151G>A
NM_001349922.1:c.-153G>A	NP_001336851.1:n.-153G>A
NR_146327.1:n.81+127G>A
NM_001349921.2:c.-2-151G>A	NP_001336850.1:n.-2-151G>A
NM_001349922.2:c.-153G>A	NP_001336851.1:n.-153G>A
NR_146327.2:n.53+127G>A