Canonical Allele Identifier: CA416614390

Gene: RPL11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.23695827A>G , CM000663.2:g.23695827A>G	GRCh38
NC_000001.10:g.24022317A>G , CM000663.1:g.24022317A>G	GRCh37
NC_000001.9:g.23894904A>G	NCBI36
NG_011741.1:g.9024A>G
NG_011741.2:g.9049A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374550.8:c.423A>G	ENSP00000363676.4:p.Ala141=
ENST00000443624.6:n.1450A>G
ENST00000458455.2:c.393A>G	ENSP00000398888.2:p.Ala131=
ENST00000467075.2:c.*522A>G	ENSP00000493634.1:n.*522A>G
ENST00000482370.2:n.420A>G
ENST00000643754.2:c.426A>G MANE Select	ENSP00000496250.1:p.Ala142=
ENST00000374550.7:c.426A>G	ENSP00000363676.3:p.Ala142=
ENST00000458455.1:c.420A>G	ENSP00000398888.1:p.Ala140=
ENST00000482370.1:n.723A>G
NM_000975.3:c.426A>G	NP_000966.2:p.Ala142=
NM_001199802.1:c.423A>G	NP_001186731.1:p.Ala141=
NM_000975.5:c.426A>G MANE Select	NP_000966.2:p.Ala142=