Canonical Allele Identifier: CA338994851
Community Standard Title: NM_000975.5(RPL11):c.508-1G>A
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23696343G>A , CM000663.2:g.23696343G>A GRCh38
NC_000001.10:g.24022833G>A , CM000663.1:g.24022833G>A GRCh37
NC_000001.9:g.23895420G>A NCBI36
NG_011741.1:g.9540G>A
NG_011741.2:g.9565G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.508-1G>A MANE Select NP_000966.2:n.508-1G>A
ENST00000643754.2:c.508-1G>A MANE Select ENSP00000496250.1:n.508-1G>A
NM_000975.3:c.508-1G>A NP_000966.2:n.508-1G>A
NM_001199802.1:c.505-1G>A NP_001186731.1:n.505-1G>A
ENST00000374550.7:c.508-1G>A ENSP00000363676.3:n.508-1G>A
ENST00000374550.8:c.505-1G>A ENSP00000363676.4:n.505-1G>A
ENST00000443624.6:n.1532-1G>A
ENST00000458455.2:c.475-1G>A ENSP00000398888.2:n.475-1G>A
ENST00000467075.2:c.*604-1G>A ENSP00000493634.1:n.*604-1G>A
ENST00000482370.1:n.805-1G>A