Canonical Allele Identifier: CA2622452959
Gene: RPL21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27254134del , CM000675.2:g.27254134del GRCh38
NC_000013.10:g.27828271del , CM000675.1:g.27828271del GRCh37
NC_000013.9:g.26726271del NCBI36
NG_046927.1:g.7580del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311549.11:c.68-86del MANE Select ENSP00000346027.4:n.68-86del
ENST00000272274.8:c.68-86del ENSP00000351021.2:n.68-86del
ENST00000311549.10:c.68-86del ENSP00000346027.4:n.68-86del
ENST00000319826.8:c.68-86del ENSP00000370574.1:n.68-86del
ENST00000326092.8:c.68-86del ENSP00000370569.1:n.68-86del
ENST00000461690.5:c.68-86del ENSP00000434298.1:n.68-86del
ENST00000466550.1:n.80-86del
ENST00000473558.5:n.304-86del
ENST00000483765.5:c.67+291del ENSP00000473246.1:n.67+291del
ENST00000493317.1:c.68-86del ENSP00000471695.1:n.68-86del
NM_000982.3:c.68-86del NP_000973.2:n.68-86del
NM_000982.4:c.68-86del MANE Select NP_000973.2:n.68-86del