Canonical Allele Identifier: CA626076705

Gene: RPL27

Linked Data

• dbSNP Id: rs1323432816
• gnomAD v2: 17-41151048-G-A
• gnomAD v3: 17-42999031-G-A
• gnomAD v4: 17-42999031-G-A
• MyVariant Identifiers: chr17:g.41151048G>A (hg19) ; chr17:g.42999031G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42999031G>A , CM000679.2:g.42999031G>A	GRCh38
NC_000017.10:g.41151048G>A , CM000679.1:g.41151048G>A	GRCh37
NC_000017.9:g.38404574G>A	NCBI36
NG_053099.1:g.5759G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.81+200G>A MANE Select	ENSP00000253788.5:n.81+200G>A
ENST00000589913.6:c.81+200G>A	ENSP00000464813.1:n.81+200G>A
ENST00000590864.2:c.82-155G>A	ENSP00000467939.2:n.82-155G>A
ENST00000253788.9:c.81+200G>A	ENSP00000253788.4:n.81+200G>A
ENST00000586277.5:c.104+119G>A
ENST00000587478.1:n.336G>A
ENST00000588830.1:c.81+200G>A	ENSP00000468468.1:n.81+200G>A
ENST00000589037.5:c.81+200G>A	ENSP00000467587.1:n.81+200G>A
ENST00000589913.5:c.81+200G>A	ENSP00000464813.1:n.81+200G>A
ENST00000593262.1:n.613G>A
NM_000988.3:c.81+200G>A	NP_000979.1:n.81+200G>A
NM_000988.5:c.81+200G>A MANE Select	NP_000979.1:n.81+200G>A
NM_001349921.1:c.81+200G>A	NP_001336850.1:n.81+200G>A
NM_001349922.1:c.81+200G>A	NP_001336851.1:n.81+200G>A
NR_146327.1:n.164+200G>A
NM_001349921.2:c.81+200G>A	NP_001336850.1:n.81+200G>A
NM_001349922.2:c.81+200G>A	NP_001336851.1:n.81+200G>A
NR_146327.2:n.136+200G>A