Canonical Allele Identifier: CA2080454182
Gene: RPL21 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27254049G= , CM000675.2:g.27254049G= GRCh38
NC_000013.10:g.27828186G= , CM000675.1:g.27828186G= GRCh37
NC_000013.9:g.26726186G= NCBI36
NG_046927.1:g.7495G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311549.11:c.68-171G= MANE Select ENSP00000346027.4:n.68-171G=
ENST00000272274.8:c.68-171G= ENSP00000351021.2:n.68-171G=
ENST00000311549.10:c.68-171G= ENSP00000346027.4:n.68-171G=
ENST00000319826.8:c.68-171G= ENSP00000370574.1:n.68-171G=
ENST00000326092.8:c.68-171G= ENSP00000370569.1:n.68-171G=
ENST00000461690.5:c.68-171G= ENSP00000434298.1:n.68-171G=
ENST00000466550.1:n.80-171G=
ENST00000473558.5:n.304-171G=
ENST00000483765.5:c.67+206G= ENSP00000473246.1:n.67+206G=
ENST00000493317.1:c.68-171G= ENSP00000471695.1:n.68-171G=
NM_000982.3:c.68-171G= NP_000973.2:n.68-171G=
NM_000982.4:c.68-171G= MANE Select NP_000973.2:n.68-171G=
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