Canonical Allele Identifier: CA497783384

Gene: RPL26

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8377645G>C , CM000679.2:g.8377645G>C	GRCh38
NC_000017.10:g.8280963G>C , CM000679.1:g.8280963G>C	GRCh37
NC_000017.9:g.8221688G>C	NCBI36
NG_031989.1:g.10603C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583011.6:c.357C>G	ENSP00000462322.1:p.Leu119=
ENST00000584164.6:c.357C>G	ENSP00000463784.1:p.Leu119=
ENST00000584906.6:c.*282C>G	ENSP00000462619.1:n.*282C>G
ENST00000648839.1:c.357C>G MANE Select	ENSP00000498177.1:p.Leu119=
ENST00000293842.9:c.357C>G	ENSP00000293842.5:p.Leu119=
ENST00000578069.1:n.337C>G
ENST00000582471.1:c.310-1541C>G	ENSP00000463847.1:n.310-1541C>G
ENST00000582485.5:c.342C>G
ENST00000582556.5:c.357C>G	ENSP00000463470.1:p.Leu119=
ENST00000583011.5:c.357C>G	ENSP00000462322.1:p.Leu119=
ENST00000584164.5:c.357C>G	ENSP00000463784.1:p.Leu119=
ENST00000584441.5:c.221C>G	ENSP00000462249.1:n.221C>G
ENST00000584906.5:c.*282C>G	ENSP00000462619.1:n.*282C>G
ENST00000585176.1:n.318C>G
NM_000987.3:c.357C>G	NP_000978.1:p.Leu119=
NM_001315530.1:c.357C>G	NP_001302459.1:p.Leu119=
NM_001315531.1:c.357C>G	NP_001302460.1:p.Leu119=
XR_934207.1:n.1673+404G>C
NM_000987.5:c.357C>G MANE Select	NP_000978.1:p.Leu119=
NM_001315530.2:c.357C>G	NP_001302459.1:p.Leu119=
NM_001315531.2:c.357C>G	NP_001302460.1:p.Leu119=