Canonical Allele Identifier: CA399675728

Gene: RPL27

Linked Data

• MyVariant Identifiers: chr17:g.41150777T>G (hg19) ; chr17:g.42998760T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998760T>G , CM000679.2:g.42998760T>G	GRCh38
NC_000017.10:g.41150777T>G , CM000679.1:g.41150777T>G	GRCh37
NC_000017.9:g.38404303T>G	NCBI36
NG_053099.1:g.5488T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000253788.12:c.10T>G MANE Select	ENSP00000253788.5:p.Phe4Val
ENST00000589913.6:c.10T>G	ENSP00000464813.1:p.Phe4Val
ENST00000590864.2:c.10T>G	ENSP00000467939.2:p.Phe4Val
ENST00000253788.9:c.10T>G	ENSP00000253788.4:p.Phe4Val
ENST00000587478.1:n.65T>G
ENST00000588830.1:c.10T>G	ENSP00000468468.1:p.Phe4Val
ENST00000589037.5:c.10T>G	ENSP00000467587.1:p.Phe4Val
ENST00000589913.5:c.10T>G	ENSP00000464813.1:p.Phe4Val
ENST00000593262.1:n.342T>G
NM_000988.3:c.10T>G	NP_000979.1:p.Phe4Val
NM_000988.5:c.10T>G MANE Select	NP_000979.1:p.Phe4Val
NM_001349921.1:c.10T>G	NP_001336850.1:p.Phe4Val
NM_001349922.1:c.10T>G	NP_001336851.1:p.Phe4Val
NR_146327.1:n.93T>G
NM_001349921.2:c.10T>G	NP_001336850.1:p.Phe4Val
NM_001349922.2:c.10T>G	NP_001336851.1:p.Phe4Val
NR_146327.2:n.65T>G