Canonical Allele Identifier: CA387623173

Gene: RPL21

Linked Data

• dbSNP Id: rs1379098665
• gnomAD v2: 13-27828388-C-G
• gnomAD v4: 13-27254251-C-G
• MyVariant Identifiers: chr13:g.27828388C>G (hg19) ; chr13:g.27254251C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254251C>G , CM000675.2:g.27254251C>G	GRCh38
NC_000013.10:g.27828388C>G , CM000675.1:g.27828388C>G	GRCh37
NC_000013.9:g.26726388C>G	NCBI36
NG_046927.1:g.7697C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.99C>G MANE Select	ENSP00000346027.4:p.Ile33Met
ENST00000272274.8:c.99C>G	ENSP00000351021.2:p.Ile33Met
ENST00000311549.10:c.99C>G	ENSP00000346027.4:p.Ile33Met
ENST00000319826.8:c.99C>G	ENSP00000370574.1:p.Ile33Met
ENST00000326092.8:c.99C>G	ENSP00000370569.1:p.Ile33Met
ENST00000461690.5:c.99C>G	ENSP00000434298.1:p.Ile33Met
ENST00000466550.1:n.111C>G
ENST00000473558.5:n.335C>G
ENST00000483765.5:c.67+408C>G	ENSP00000473246.1:n.67+408C>G
ENST00000493317.1:c.99C>G	ENSP00000471695.1:p.Ile33Met
NM_000982.3:c.99C>G	NP_000973.2:p.Ile33Met
NM_000982.4:c.99C>G MANE Select	NP_000973.2:p.Ile33Met