Canonical Allele Identifier: CA2080454180
Gene: RPL21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27254044_27254046delinsGGA , CM000675.2:g.27254044_27254046delinsGGA GRCh38
NC_000013.10:g.27828181_27828183delinsGGA , CM000675.1:g.27828181_27828183delinsGGA GRCh37
NC_000013.9:g.26726181_26726183delinsGGA NCBI36
NG_046927.1:g.7490_7492delinsGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000311549.11:c.68-176_68-174delinsGGA MANE Select ENSP00000346027.4:n.68-176_68-174delinsGGA
ENST00000272274.8:c.68-176_68-174delinsGGA ENSP00000351021.2:n.68-176_68-174delinsGGA
ENST00000311549.10:c.68-176_68-174delinsGGA ENSP00000346027.4:n.68-176_68-174delinsGGA
ENST00000319826.8:c.68-176_68-174delinsGGA ENSP00000370574.1:n.68-176_68-174delinsGGA
ENST00000326092.8:c.68-176_68-174delinsGGA ENSP00000370569.1:n.68-176_68-174delinsGGA
ENST00000461690.5:c.68-176_68-174delinsGGA ENSP00000434298.1:n.68-176_68-174delinsGGA
ENST00000466550.1:n.80-176_80-174delinsGGA
ENST00000473558.5:n.304-176_304-174delinsGGA
ENST00000483765.5:c.67+201_67+203delinsGGA ENSP00000473246.1:n.67+201_67+203delinsGGA
ENST00000493317.1:c.68-176_68-174delinsGGA ENSP00000471695.1:n.68-176_68-174delinsGGA
NM_000982.3:c.68-176_68-174delinsGGA NP_000973.2:n.68-176_68-174delinsGGA
NM_000982.4:c.68-176_68-174delinsGGA MANE Select NP_000973.2:n.68-176_68-174delinsGGA