Canonical Allele Identifier: CA684151
Community Standard Title: NM_000975.5(RPL11):c.14A>G (p.Gln5Arg)
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23692616A>G , CM000663.2:g.23692616A>G GRCh38
NC_000001.10:g.24019106A>G , CM000663.1:g.24019106A>G GRCh37
NC_000001.9:g.23891693A>G NCBI36
NG_011741.1:g.5813A>G
NG_011741.2:g.5838A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.14A>G MANE Select NP_000966.2:p.Gln5Arg
ENST00000643754.2:c.14A>G MANE Select ENSP00000496250.1:p.Gln5Arg
NM_000975.3:c.14A>G NP_000966.2:p.Gln5Arg
NM_001199802.1:c.11A>G NP_001186731.1:p.Gln4Arg
ENST00000374550.7:c.14A>G ENSP00000363676.3:p.Gln5Arg
ENST00000374550.8:c.11A>G ENSP00000363676.4:p.Gln4Arg
ENST00000443624.5:c.8A>G ENSP00000390839.1:p.Gln3Arg
ENST00000443624.6:n.32A>G
ENST00000458455.1:c.8A>G ENSP00000398888.1:p.Gln3Arg
ENST00000458455.2:c.-20A>G ENSP00000398888.2:n.-20A>G
ENST00000467075.1:n.234A>G
ENST00000467075.2:c.*110A>G ENSP00000493634.1:n.*110A>G
ENST00000482370.1:n.311A>G
ENST00000482370.2:n.8A>G