Canonical Allele Identifier: CA398014559

Gene: RPL26

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8379819G>A , CM000679.2:g.8379819G>A	GRCh38
NC_000017.10:g.8283137G>A , CM000679.1:g.8283137G>A	GRCh37
NC_000017.9:g.8223862G>A	NCBI36
NG_031989.1:g.8429C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583011.6:c.286C>T	ENSP00000462322.1:p.His96Tyr
ENST00000584164.6:c.286C>T	ENSP00000463784.1:p.His96Tyr
ENST00000584343.6:c.286C>T	ENSP00000464239.1:p.His96Tyr
ENST00000584906.6:c.*211C>T	ENSP00000462619.1:n.*211C>T
ENST00000648839.1:c.286C>T MANE Select	ENSP00000498177.1:p.His96Tyr
ENST00000293842.9:c.286C>T	ENSP00000293842.5:p.His96Tyr
ENST00000578069.1:n.266C>T
ENST00000578812.5:c.286C>T	ENSP00000463910.1:p.His96Tyr
ENST00000582471.1:c.286C>T	ENSP00000463847.1:p.His96Tyr
ENST00000582485.5:c.285C>T
ENST00000582556.5:c.286C>T	ENSP00000463470.1:p.His96Tyr
ENST00000583011.5:c.286C>T	ENSP00000462322.1:p.His96Tyr
ENST00000583515.1:c.286C>T	ENSP00000463021.1:p.His96Tyr
ENST00000584164.5:c.286C>T	ENSP00000463784.1:p.His96Tyr
ENST00000584343.5:c.286C>T	ENSP00000464239.1:p.His96Tyr
ENST00000584441.5:c.118C>T	ENSP00000462249.1:p.His40Tyr
ENST00000584906.5:c.*211C>T	ENSP00000462619.1:n.*211C>T
ENST00000585176.1:n.247C>T
NM_000987.3:c.286C>T	NP_000978.1:p.His96Tyr
NM_001315530.1:c.286C>T	NP_001302459.1:p.His96Tyr
NM_001315531.1:c.286C>T	NP_001302460.1:p.His96Tyr
XR_934207.1:n.1674-1226G>A
NM_000987.5:c.286C>T MANE Select	NP_000978.1:p.His96Tyr
NM_001315530.2:c.286C>T	NP_001302459.1:p.His96Tyr
NM_001315531.2:c.286C>T	NP_001302460.1:p.His96Tyr