Canonical Allele Identifier: CA19285783
Community Standard Title: NM_000975.5(RPL11):c.158-7C>G
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23693800C>G , CM000663.2:g.23693800C>G GRCh38
NC_000001.10:g.24020290C>G , CM000663.1:g.24020290C>G GRCh37
NC_000001.9:g.23892877C>G NCBI36
NG_011741.1:g.6997C>G
NG_011741.2:g.7022C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.158-7C>G MANE Select NP_000966.2:n.158-7C>G
ENST00000643754.2:c.158-7C>G MANE Select ENSP00000496250.1:n.158-7C>G
NM_000975.3:c.158-7C>G NP_000966.2:n.158-7C>G
NM_001199802.1:c.155-7C>G NP_001186731.1:n.155-7C>G
ENST00000374550.7:c.158-7C>G ENSP00000363676.3:n.158-7C>G
ENST00000374550.8:c.155-7C>G ENSP00000363676.4:n.155-7C>G
ENST00000443624.5:c.152-7C>G ENSP00000390839.1:n.152-7C>G
ENST00000443624.6:n.176-7C>G
ENST00000458455.1:c.152-7C>G ENSP00000398888.1:n.152-7C>G
ENST00000458455.2:c.125-7C>G ENSP00000398888.2:n.125-7C>G
ENST00000467075.2:c.*254-7C>G ENSP00000493634.1:n.*254-7C>G
ENST00000482370.1:n.455-7C>G
ENST00000482370.2:n.152-7C>G