Canonical Allele Identifier: CA338991250
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23692609C>G , CM000663.2:g.23692609C>G GRCh38
NC_000001.10:g.24019099C>G , CM000663.1:g.24019099C>G GRCh37
NC_000001.9:g.23891686C>G NCBI36
NG_011741.1:g.5806C>G
NG_011741.2:g.5831C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374550.8:c.7-3C>G ENSP00000363676.4:n.7-3C>G
ENST00000443624.6:n.25C>G
ENST00000458455.2:c.-27C>G ENSP00000398888.2:n.-27C>G
ENST00000467075.2:c.*103C>G ENSP00000493634.1:n.*103C>G
ENST00000482370.2:n.1C>G
ENST00000643754.2:c.7C>G MANE Select ENSP00000496250.1:p.Gln3Glu
ENST00000374550.7:c.7C>G ENSP00000363676.3:p.Gln3Glu
ENST00000443624.5:c.1C>G ENSP00000390839.1:p.Gln1Glu
ENST00000458455.1:c.1C>G ENSP00000398888.1:p.Gln1Glu
ENST00000467075.1:n.227C>G
ENST00000482370.1:n.304C>G
NM_000975.3:c.7C>G NP_000966.2:p.Gln3Glu
NM_001199802.1:c.7-3C>G NP_001186731.1:n.7-3C>G
NM_000975.5:c.7C>G MANE Select NP_000966.2:p.Gln3Glu