Canonical Allele Identifier: CA2825002660

Gene: RPL26

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8382317T>C , CM000679.2:g.8382317T>C	GRCh38
NC_000017.10:g.8285635T>C , CM000679.1:g.8285635T>C	GRCh37
NC_000017.9:g.8226360T>C	NCBI36
NG_031989.1:g.5931A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000987.5:c.-5-2A>G MANE Select	NP_000978.1:n.-5-2A>G
ENST00000648839.1:c.-5-2A>G MANE Select	ENSP00000498177.1:n.-5-2A>G
NM_000987.3:c.-5-2A>G	NP_000978.1:n.-5-2A>G
NM_001315530.1:c.-5-2A>G	NP_001302459.1:n.-5-2A>G
NM_001315530.2:c.-5-2A>G	NP_001302459.1:n.-5-2A>G
NM_001315531.1:c.-5-2A>G	NP_001302460.1:n.-5-2A>G
NM_001315531.2:c.-5-2A>G	NP_001302460.1:n.-5-2A>G
ENST00000293842.9:c.-5-2A>G	ENSP00000293842.5:n.-5-2A>G
ENST00000578115.1:n.38-2A>G
ENST00000578812.5:c.-5-2A>G	ENSP00000463910.1:n.-5-2A>G
ENST00000582471.1:c.-5-2A>G	ENSP00000463847.1:n.-5-2A>G
ENST00000582556.5:c.-5-2A>G	ENSP00000463470.1:n.-5-2A>G
ENST00000583011.5:c.-7A>G	ENSP00000462322.1:n.-7A>G
ENST00000583011.6:c.-7A>G	ENSP00000462322.1:n.-7A>G
ENST00000583515.1:c.-7A>G	ENSP00000463021.1:n.-7A>G
ENST00000584164.5:c.-5-2A>G	ENSP00000463784.1:n.-5-2A>G
ENST00000584164.6:c.-5-2A>G	ENSP00000463784.1:n.-5-2A>G
ENST00000584343.5:c.-5-2A>G	ENSP00000464239.1:n.-5-2A>G
ENST00000584343.6:c.-5-2A>G	ENSP00000464239.1:n.-5-2A>G
ENST00000585176.1:n.37-227A>G