Canonical Allele Identifier: CA497784444

Gene: RPL26

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8382296G>C , CM000679.2:g.8382296G>C	GRCh38
NC_000017.10:g.8285614G>C , CM000679.1:g.8285614G>C	GRCh37
NC_000017.9:g.8226339G>C	NCBI36
NG_031989.1:g.5952C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583011.6:c.15C>G	ENSP00000462322.1:p.Pro5=
ENST00000584164.6:c.15C>G	ENSP00000463784.1:p.Pro5=
ENST00000584343.6:c.15C>G	ENSP00000464239.1:p.Pro5=
ENST00000584906.6:c.15C>G	ENSP00000462619.1:p.Pro5=
ENST00000648839.1:c.15C>G MANE Select	ENSP00000498177.1:p.Pro5=
ENST00000293842.9:c.15C>G	ENSP00000293842.5:p.Pro5=
ENST00000578115.1:n.57C>G
ENST00000578812.5:c.15C>G	ENSP00000463910.1:p.Pro5=
ENST00000582471.1:c.15C>G	ENSP00000463847.1:p.Pro5=
ENST00000582485.5:c.14C>G
ENST00000582556.5:c.15C>G	ENSP00000463470.1:p.Pro5=
ENST00000583011.5:c.15C>G	ENSP00000462322.1:p.Pro5=
ENST00000583515.1:c.15C>G	ENSP00000463021.1:p.Pro5=
ENST00000584164.5:c.15C>G	ENSP00000463784.1:p.Pro5=
ENST00000584343.5:c.15C>G	ENSP00000464239.1:p.Pro5=
ENST00000584906.5:c.15C>G	ENSP00000462619.1:p.Pro5=
ENST00000585176.1:n.37-206C>G
NM_000987.3:c.15C>G	NP_000978.1:p.Pro5=
NM_001315530.1:c.15C>G	NP_001302459.1:p.Pro5=
NM_001315531.1:c.15C>G	NP_001302460.1:p.Pro5=
NM_000987.5:c.15C>G MANE Select	NP_000978.1:p.Pro5=
NM_001315530.2:c.15C>G	NP_001302459.1:p.Pro5=
NM_001315531.2:c.15C>G	NP_001302460.1:p.Pro5=