Canonical Allele Identifier: CA338993342
Community Standard Title: NM_000975.5(RPL11):c.328C>T (p.Gln110Ter)
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23694723C>T , CM000663.2:g.23694723C>T GRCh38
NC_000001.10:g.24021213C>T , CM000663.1:g.24021213C>T GRCh37
NC_000001.9:g.23893800C>T NCBI36
NG_011741.1:g.7920C>T
NG_011741.2:g.7945C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.328C>T MANE Select NP_000966.2:p.Gln110Ter
ENST00000643754.2:c.328C>T MANE Select ENSP00000496250.1:p.Gln110Ter
NM_000975.3:c.328C>T NP_000966.2:p.Gln110Ter
NM_001199802.1:c.325C>T NP_001186731.1:p.Gln109Ter
ENST00000374550.7:c.328C>T ENSP00000363676.3:p.Gln110Ter
ENST00000374550.8:c.325C>T ENSP00000363676.4:p.Gln109Ter
ENST00000443624.5:c.322C>T ENSP00000390839.1:p.Gln108Ter
ENST00000443624.6:n.346C>T
ENST00000458455.1:c.322C>T ENSP00000398888.1:p.Gln108Ter
ENST00000458455.2:c.295C>T ENSP00000398888.2:p.Gln99Ter
ENST00000467075.2:c.*424C>T ENSP00000493634.1:n.*424C>T
ENST00000482370.1:n.625C>T
ENST00000482370.2:n.322C>T