Canonical Allele Identifier: CA2080454178
Gene: RPL21 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27254036T= , CM000675.2:g.27254036T= GRCh38
NC_000013.10:g.27828173T= , CM000675.1:g.27828173T= GRCh37
NC_000013.9:g.26726173T= NCBI36
NG_046927.1:g.7482T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000311549.11:c.68-184T= MANE Select ENSP00000346027.4:n.68-184T=
ENST00000272274.8:c.68-184T= ENSP00000351021.2:n.68-184T=
ENST00000311549.10:c.68-184T= ENSP00000346027.4:n.68-184T=
ENST00000319826.8:c.68-184T= ENSP00000370574.1:n.68-184T=
ENST00000326092.8:c.68-184T= ENSP00000370569.1:n.68-184T=
ENST00000461690.5:c.68-184T= ENSP00000434298.1:n.68-184T=
ENST00000466550.1:n.80-184T=
ENST00000473558.5:n.304-184T=
ENST00000483765.5:c.67+193T= ENSP00000473246.1:n.67+193T=
ENST00000493317.1:c.68-184T= ENSP00000471695.1:n.68-184T=
NM_000982.3:c.68-184T= NP_000973.2:n.68-184T=
NM_000982.4:c.68-184T= MANE Select NP_000973.2:n.68-184T=
Search 100 bp 5'
Search 100 bp 3'