Canonical Allele Identifier: CA497783364

Gene: RPL26

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8377633G>A , CM000679.2:g.8377633G>A	GRCh38
NC_000017.10:g.8280951G>A , CM000679.1:g.8280951G>A	GRCh37
NC_000017.9:g.8221676G>A	NCBI36
NG_031989.1:g.10615C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583011.6:c.369C>T	ENSP00000462322.1:p.Ala123=
ENST00000584164.6:c.369C>T	ENSP00000463784.1:p.Ala123=
ENST00000584906.6:c.*294C>T	ENSP00000462619.1:n.*294C>T
ENST00000648839.1:c.369C>T MANE Select	ENSP00000498177.1:p.Ala123=
ENST00000293842.9:c.369C>T	ENSP00000293842.5:p.Ala123=
ENST00000578069.1:n.349C>T
ENST00000582471.1:c.310-1529C>T	ENSP00000463847.1:n.310-1529C>T
ENST00000582485.5:c.354C>T
ENST00000582556.5:c.369C>T	ENSP00000463470.1:p.Ala123=
ENST00000583011.5:c.369C>T	ENSP00000462322.1:p.Ala123=
ENST00000584164.5:c.369C>T	ENSP00000463784.1:p.Ala123=
ENST00000584441.5:c.233C>T	ENSP00000462249.1:n.233C>T
ENST00000584906.5:c.*294C>T	ENSP00000462619.1:n.*294C>T
ENST00000585176.1:n.330C>T
NM_000987.3:c.369C>T	NP_000978.1:p.Ala123=
NM_001315530.1:c.369C>T	NP_001302459.1:p.Ala123=
NM_001315531.1:c.369C>T	NP_001302460.1:p.Ala123=
XR_934207.1:n.1673+392G>A
NM_000987.5:c.369C>T MANE Select	NP_000978.1:p.Ala123=
NM_001315530.2:c.369C>T	NP_001302459.1:p.Ala123=
NM_001315531.2:c.369C>T	NP_001302460.1:p.Ala123=