Canonical Allele Identifier: CA387623291
Gene: RPL21 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27254276A>C , CM000675.2:g.27254276A>C GRCh38
NC_000013.10:g.27828413A>C , CM000675.1:g.27828413A>C GRCh37
NC_000013.9:g.26726413A>C NCBI36
NG_046927.1:g.7722A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000311549.11:c.124A>C MANE Select ENSP00000346027.4:p.Ile42Leu
ENST00000272274.8:c.124A>C ENSP00000351021.2:p.Ile42Leu
ENST00000311549.10:c.124A>C ENSP00000346027.4:p.Ile42Leu
ENST00000319826.8:c.124A>C ENSP00000370574.1:p.Ile42Leu
ENST00000326092.8:c.124A>C ENSP00000370569.1:p.Ile42Leu
ENST00000461690.5:c.124A>C ENSP00000434298.1:p.Ile42Leu
ENST00000466550.1:n.136A>C
ENST00000473558.5:n.360A>C
ENST00000483765.5:c.67+433A>C ENSP00000473246.1:n.67+433A>C
ENST00000493317.1:c.124A>C ENSP00000471695.1:p.Ile42Leu
NM_000982.3:c.124A>C NP_000973.2:p.Ile42Leu
NM_000982.4:c.124A>C MANE Select NP_000973.2:p.Ile42Leu