Canonical Allele Identifier: CA500120588

Gene: RPL27

Linked Data

• MyVariant Identifiers: chr17:g.41150833A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998816A>G , CM000679.2:g.42998816A>G	GRCh38
NC_000017.10:g.41150833A>G , CM000679.1:g.41150833A>G	GRCh37
NC_000017.9:g.38404359A>G	NCBI36
NG_053099.1:g.5544A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.66A>G MANE Select	ENSP00000253788.5:p.Lys22=
ENST00000589913.6:c.66A>G	ENSP00000464813.1:p.Lys22=
ENST00000590864.2:c.66A>G	ENSP00000467939.2:p.Lys22=
ENST00000253788.9:c.66A>G	ENSP00000253788.4:p.Lys22=
ENST00000586277.5:c.8A>G
ENST00000587478.1:n.121A>G
ENST00000588830.1:c.66A>G	ENSP00000468468.1:p.Lys22=
ENST00000589037.5:c.66A>G	ENSP00000467587.1:p.Lys22=
ENST00000589913.5:c.66A>G	ENSP00000464813.1:p.Lys22=
ENST00000593262.1:n.398A>G
NM_000988.3:c.66A>G	NP_000979.1:p.Lys22=
NM_000988.5:c.66A>G MANE Select	NP_000979.1:p.Lys22=
NM_001349921.1:c.66A>G	NP_001336850.1:p.Lys22=
NM_001349922.1:c.66A>G	NP_001336851.1:p.Lys22=
NR_146327.1:n.149A>G
NM_001349921.2:c.66A>G	NP_001336850.1:p.Lys22=
NM_001349922.2:c.66A>G	NP_001336851.1:p.Lys22=
NR_146327.2:n.121A>G