Canonical Allele Identifier: CA2638053009

Gene: RPL27

Linked Data

• gnomAD v4: 17-42998485-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998485T>A , CM000679.2:g.42998485T>A	GRCh38
NC_000017.10:g.41150502T>A , CM000679.1:g.41150502T>A	GRCh37
NC_000017.9:g.38404028T>A	NCBI36
NG_053099.1:g.5213T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.-3+14T>A MANE Select	ENSP00000253788.5:n.-3+14T>A
ENST00000589913.6:c.-266T>A	ENSP00000464813.1:n.-266T>A
ENST00000253788.9:c.-3+14T>A	ENSP00000253788.4:n.-3+14T>A
ENST00000587478.1:n.53+14T>A
ENST00000588830.1:c.-3+14T>A	ENSP00000468468.1:n.-3+14T>A
ENST00000589037.5:c.-3+70T>A	ENSP00000467587.1:n.-3+70T>A
ENST00000589913.5:c.-266T>A	ENSP00000464813.1:n.-266T>A
ENST00000593262.1:n.67T>A
NM_000988.3:c.-3+14T>A	NP_000979.1:n.-3+14T>A
NM_000988.5:c.-3+14T>A MANE Select	NP_000979.1:n.-3+14T>A
NM_001349921.1:c.-3+70T>A	NP_001336850.1:n.-3+70T>A
NM_001349922.1:c.-266T>A	NP_001336851.1:n.-266T>A
NR_146327.1:n.81+14T>A
NM_001349921.2:c.-3+70T>A	NP_001336850.1:n.-3+70T>A
NM_001349922.2:c.-266T>A	NP_001336851.1:n.-266T>A
NR_146327.2:n.53+14T>A