Canonical Allele Identifier: CA399675905

Gene: RPL27

Linked Data

• ClinVar Variation Id: 2406638
• ClinVar RCV Id: RCV004239819
• MyVariant Identifiers: chr17:g.41150828C>G (hg19) ; chr17:g.42998811C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998811C>G , CM000679.2:g.42998811C>G	GRCh38
NC_000017.10:g.41150828C>G , CM000679.1:g.41150828C>G	GRCh37
NC_000017.9:g.38404354C>G	NCBI36
NG_053099.1:g.5539C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.61C>G MANE Select	ENSP00000253788.5:p.Arg21Gly
ENST00000589913.6:c.61C>G	ENSP00000464813.1:p.Arg21Gly
ENST00000590864.2:c.61C>G	ENSP00000467939.2:p.Arg21Gly
ENST00000253788.9:c.61C>G	ENSP00000253788.4:p.Arg21Gly
ENST00000586277.5:c.3C>G
ENST00000587478.1:n.116C>G
ENST00000588830.1:c.61C>G	ENSP00000468468.1:p.Arg21Gly
ENST00000589037.5:c.61C>G	ENSP00000467587.1:p.Arg21Gly
ENST00000589913.5:c.61C>G	ENSP00000464813.1:p.Arg21Gly
ENST00000593262.1:n.393C>G
NM_000988.3:c.61C>G	NP_000979.1:p.Arg21Gly
NM_000988.5:c.61C>G MANE Select	NP_000979.1:p.Arg21Gly
NM_001349921.1:c.61C>G	NP_001336850.1:p.Arg21Gly
NM_001349922.1:c.61C>G	NP_001336851.1:p.Arg21Gly
NR_146327.1:n.144C>G
NM_001349921.2:c.61C>G	NP_001336850.1:p.Arg21Gly
NM_001349922.2:c.61C>G	NP_001336851.1:p.Arg21Gly
NR_146327.2:n.116C>G