Canonical Allele Identifier: CA2580061502
Community Standard Title: NM_000975.5(RPL11):c.33del (p.Met12CysfsTer22)
Gene: RPL11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.23692635del , CM000663.2:g.23692635del GRCh38
NC_000001.10:g.24019125del , CM000663.1:g.24019125del GRCh37
NC_000001.9:g.23891712del NCBI36
NG_011741.1:g.5832del
NG_011741.2:g.5857del

Transcript Alleles

HGVS Amino-acid Change
NM_000975.5:c.33del MANE Select NP_000966.2:p.Met12CysfsTer22
ENST00000643754.2:c.33del MANE Select ENSP00000496250.1:p.Met12CysfsTer22
NM_000975.3:c.33del NP_000966.2:p.Met12CysfsTer22
NM_001199802.1:c.30del NP_001186731.1:p.Met11CysfsTer22
ENST00000374550.7:c.33del ENSP00000363676.3:p.Met12CysfsTer22
ENST00000374550.8:c.30del ENSP00000363676.4:p.Met11CysfsTer22
ENST00000443624.5:c.27del ENSP00000390839.1:p.Met10CysfsTer22
ENST00000443624.6:n.51del
ENST00000458455.1:c.27del ENSP00000398888.1:p.Met10CysfsTer22
ENST00000458455.2:c.-1del ENSP00000398888.2:n.-1del
ENST00000467075.1:n.253del
ENST00000467075.2:c.*129del ENSP00000493634.1:n.*129del
ENST00000482370.1:n.330del
ENST00000482370.2:n.27del