Canonical Allele Identifier: CA338991852
Community Standard Title: NM_000975.5(RPL11):c.121G>T (p.Glu41Ter)
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23692723G>T , CM000663.2:g.23692723G>T GRCh38
NC_000001.10:g.24019213G>T , CM000663.1:g.24019213G>T GRCh37
NC_000001.9:g.23891800G>T NCBI36
NG_011741.1:g.5920G>T
NG_011741.2:g.5945G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.121G>T MANE Select NP_000966.2:p.Glu41Ter
ENST00000643754.2:c.121G>T MANE Select ENSP00000496250.1:p.Glu41Ter
NM_000975.3:c.121G>T NP_000966.2:p.Glu41Ter
NM_001199802.1:c.118G>T NP_001186731.1:p.Glu40Ter
ENST00000374550.7:c.121G>T ENSP00000363676.3:p.Glu41Ter
ENST00000374550.8:c.118G>T ENSP00000363676.4:p.Glu40Ter
ENST00000443624.5:c.115G>T ENSP00000390839.1:p.Glu39Ter
ENST00000443624.6:n.139G>T
ENST00000458455.1:c.115G>T ENSP00000398888.1:p.Glu39Ter
ENST00000458455.2:c.88G>T ENSP00000398888.2:p.Glu30Ter
ENST00000467075.1:n.341G>T
ENST00000467075.2:c.*217G>T ENSP00000493634.1:n.*217G>T
ENST00000482370.1:n.418G>T
ENST00000482370.2:n.115G>T