Canonical Allele Identifier: CA399675854

Gene: RPL27

Linked Data

• MyVariant Identifiers: chr17:g.41150814G>T (hg19) ; chr17:g.42998797G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.42998797G>T , CM000679.2:g.42998797G>T	GRCh38
NC_000017.10:g.41150814G>T , CM000679.1:g.41150814G>T	GRCh37
NC_000017.9:g.38404340G>T	NCBI36
NG_053099.1:g.5525G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253788.12:c.47G>T MANE Select	ENSP00000253788.5:p.Gly16Val
ENST00000589913.6:c.47G>T	ENSP00000464813.1:p.Gly16Val
ENST00000590864.2:c.47G>T	ENSP00000467939.2:p.Gly16Val
ENST00000253788.9:c.47G>T	ENSP00000253788.4:p.Gly16Val
ENST00000587478.1:n.102G>T
ENST00000588830.1:c.47G>T	ENSP00000468468.1:p.Gly16Val
ENST00000589037.5:c.47G>T	ENSP00000467587.1:p.Gly16Val
ENST00000589913.5:c.47G>T	ENSP00000464813.1:p.Gly16Val
ENST00000593262.1:n.379G>T
NM_000988.3:c.47G>T	NP_000979.1:p.Gly16Val
NM_000988.5:c.47G>T MANE Select	NP_000979.1:p.Gly16Val
NM_001349921.1:c.47G>T	NP_001336850.1:p.Gly16Val
NM_001349922.1:c.47G>T	NP_001336851.1:p.Gly16Val
NR_146327.1:n.130G>T
NM_001349921.2:c.47G>T	NP_001336850.1:p.Gly16Val
NM_001349922.2:c.47G>T	NP_001336851.1:p.Gly16Val
NR_146327.2:n.102G>T