Canonical Allele Identifier: CA684269
Community Standard Title: NM_000975.5(RPL11):c.396+9A>G
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23694800A>G , CM000663.2:g.23694800A>G GRCh38
NC_000001.10:g.24021290A>G , CM000663.1:g.24021290A>G GRCh37
NC_000001.9:g.23893877A>G NCBI36
NG_011741.1:g.7997A>G
NG_011741.2:g.8022A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.396+9A>G MANE Select NP_000966.2:n.396+9A>G
ENST00000643754.2:c.396+9A>G MANE Select ENSP00000496250.1:n.396+9A>G
NM_000975.3:c.396+9A>G NP_000966.2:n.396+9A>G
NM_001199802.1:c.393+9A>G NP_001186731.1:n.393+9A>G
ENST00000374550.7:c.396+9A>G ENSP00000363676.3:n.396+9A>G
ENST00000374550.8:c.393+9A>G ENSP00000363676.4:n.393+9A>G
ENST00000443624.5:c.399A>G ENSP00000390839.1:n.399A>G
ENST00000443624.6:n.423A>G
ENST00000458455.1:c.390+9A>G ENSP00000398888.1:n.390+9A>G
ENST00000458455.2:c.363+9A>G ENSP00000398888.2:n.363+9A>G
ENST00000467075.2:c.*492+9A>G ENSP00000493634.1:n.*492+9A>G
ENST00000482370.1:n.693+9A>G
ENST00000482370.2:n.390+9A>G