Canonical Allele Identifier: CA399675880

Gene: RPL27

Linked Data

• MyVariant Identifiers: chr17:g.41150822T>A (hg19) ; chr17:g.42998805T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998805T>A , CM000679.2:g.42998805T>A	GRCh38
NC_000017.10:g.41150822T>A , CM000679.1:g.41150822T>A	GRCh37
NC_000017.9:g.38404348T>A	NCBI36
NG_053099.1:g.5533T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.55T>A MANE Select	ENSP00000253788.5:p.Ser19Thr
ENST00000589913.6:c.55T>A	ENSP00000464813.1:p.Ser19Thr
ENST00000590864.2:c.55T>A	ENSP00000467939.2:p.Ser19Thr
ENST00000253788.9:c.55T>A	ENSP00000253788.4:p.Ser19Thr
ENST00000587478.1:n.110T>A
ENST00000588830.1:c.55T>A	ENSP00000468468.1:p.Ser19Thr
ENST00000589037.5:c.55T>A	ENSP00000467587.1:p.Ser19Thr
ENST00000589913.5:c.55T>A	ENSP00000464813.1:p.Ser19Thr
ENST00000593262.1:n.387T>A
NM_000988.3:c.55T>A	NP_000979.1:p.Ser19Thr
NM_000988.5:c.55T>A MANE Select	NP_000979.1:p.Ser19Thr
NM_001349921.1:c.55T>A	NP_001336850.1:p.Ser19Thr
NM_001349922.1:c.55T>A	NP_001336851.1:p.Ser19Thr
NR_146327.1:n.138T>A
NM_001349921.2:c.55T>A	NP_001336850.1:p.Ser19Thr
NM_001349922.2:c.55T>A	NP_001336851.1:p.Ser19Thr
NR_146327.2:n.110T>A