Canonical Allele Identifier: CA398012520

Gene: RPL26

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8377620C>T , CM000679.2:g.8377620C>T	GRCh38
NC_000017.10:g.8280938C>T , CM000679.1:g.8280938C>T	GRCh37
NC_000017.9:g.8221663C>T	NCBI36
NG_031989.1:g.10628G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583011.6:c.382G>A	ENSP00000462322.1:p.Val128Ile
ENST00000584164.6:c.382G>A	ENSP00000463784.1:p.Val128Ile
ENST00000584906.6:c.*307G>A	ENSP00000462619.1:n.*307G>A
ENST00000648839.1:c.382G>A MANE Select	ENSP00000498177.1:p.Val128Ile
ENST00000293842.9:c.382G>A	ENSP00000293842.5:p.Val128Ile
ENST00000578069.1:n.362G>A
ENST00000582471.1:c.310-1516G>A	ENSP00000463847.1:n.310-1516G>A
ENST00000582485.5:c.367G>A
ENST00000582556.5:c.382G>A	ENSP00000463470.1:p.Val128Ile
ENST00000583011.5:c.382G>A	ENSP00000462322.1:p.Val128Ile
ENST00000584164.5:c.382G>A	ENSP00000463784.1:p.Val128Ile
ENST00000584441.5:c.246G>A	ENSP00000462249.1:n.246G>A
ENST00000584906.5:c.*307G>A	ENSP00000462619.1:n.*307G>A
ENST00000585176.1:n.343G>A
NM_000987.3:c.382G>A	NP_000978.1:p.Val128Ile
NM_001315530.1:c.382G>A	NP_001302459.1:p.Val128Ile
NM_001315531.1:c.382G>A	NP_001302460.1:p.Val128Ile
XR_934207.1:n.1673+379C>T
NM_000987.5:c.382G>A MANE Select	NP_000978.1:p.Val128Ile
NM_001315530.2:c.382G>A	NP_001302459.1:p.Val128Ile
NM_001315531.2:c.382G>A	NP_001302460.1:p.Val128Ile