Canonical Allele Identifier: CA497783293
Community Standard Title: NM_000987.5(RPL26):c.426G>A (p.Lys142=)
Gene: RPL26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8377576C>T , CM000679.2:g.8377576C>T GRCh38
NC_000017.10:g.8280894C>T , CM000679.1:g.8280894C>T GRCh37
NC_000017.9:g.8221619C>T NCBI36
NG_031989.1:g.10672G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000987.5:c.426G>A MANE Select NP_000978.1:p.Lys142=
ENST00000648839.1:c.426G>A MANE Select ENSP00000498177.1:p.Lys142=
NM_000987.3:c.426G>A NP_000978.1:p.Lys142=
NM_001315530.1:c.426G>A NP_001302459.1:p.Lys142=
NM_001315530.2:c.426G>A NP_001302459.1:p.Lys142=
NM_001315531.1:c.426G>A NP_001302460.1:p.Lys142=
NM_001315531.2:c.426G>A NP_001302460.1:p.Lys142=
ENST00000293842.9:c.426G>A ENSP00000293842.5:p.Lys142=
ENST00000578069.1:n.406G>A
ENST00000582471.1:c.310-1472G>A ENSP00000463847.1:n.310-1472G>A
ENST00000582485.5:c.411G>A
ENST00000582556.5:c.426G>A ENSP00000463470.1:p.Lys142=
ENST00000583011.5:c.426G>A ENSP00000462322.1:p.Lys142=
ENST00000583011.6:c.426G>A ENSP00000462322.1:p.Lys142=
ENST00000584164.5:c.426G>A ENSP00000463784.1:p.Lys142=
ENST00000584164.6:c.426G>A ENSP00000463784.1:p.Lys142=
ENST00000584441.5:c.290G>A ENSP00000462249.1:n.290G>A
ENST00000584906.5:c.*351G>A ENSP00000462619.1:n.*351G>A
ENST00000584906.6:c.*351G>A ENSP00000462619.1:n.*351G>A
XR_934207.1:n.1673+335C>T