Canonical Allele Identifier: CA2798599728
Gene: RPL21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27254341T>G , CM000675.2:g.27254341T>G GRCh38
NC_000013.10:g.27828478T>G , CM000675.1:g.27828478T>G GRCh37
NC_000013.9:g.26726478T>G NCBI36
NG_046927.1:g.7787T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000311549.11:c.129+60T>G MANE Select ENSP00000346027.4:n.129+60T>G
ENST00000272274.8:c.129+60T>G ENSP00000351021.2:n.129+60T>G
ENST00000311549.10:c.129+60T>G ENSP00000346027.4:n.129+60T>G
ENST00000319826.8:c.129+60T>G ENSP00000370574.1:n.129+60T>G
ENST00000326092.8:c.129+60T>G ENSP00000370569.1:n.129+60T>G
ENST00000461690.5:c.129+60T>G ENSP00000434298.1:n.129+60T>G
ENST00000466550.1:n.141+60T>G
ENST00000473558.5:n.425T>G
ENST00000483765.5:c.67+498T>G ENSP00000473246.1:n.67+498T>G
ENST00000493317.1:c.129+60T>G ENSP00000471695.1:n.129+60T>G
NM_000982.3:c.129+60T>G NP_000973.2:n.129+60T>G
NM_000982.4:c.129+60T>G MANE Select NP_000973.2:n.129+60T>G