Canonical Allele Identifier: CA919233601

Gene: RPL21

Linked Data

• dbSNP Id: rs1593261172
• gnomAD v3: 13-27254021-GTA-G
• gnomAD v4: 13-27254021-GTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254023_27254024del , CM000675.2:g.27254023_27254024del	GRCh38
NC_000013.10:g.27828160_27828161del , CM000675.1:g.27828160_27828161del	GRCh37
NC_000013.9:g.26726160_26726161del	NCBI36
NG_046927.1:g.7469_7470del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.67+180_67+181del MANE Select	ENSP00000346027.4:n.67+180_67+181del
ENST00000272274.8:c.67+180_67+181del	ENSP00000351021.2:n.67+180_67+181del
ENST00000311549.10:c.67+180_67+181del	ENSP00000346027.4:n.67+180_67+181del
ENST00000319826.8:c.67+180_67+181del	ENSP00000370574.1:n.67+180_67+181del
ENST00000326092.8:c.67+180_67+181del	ENSP00000370569.1:n.67+180_67+181del
ENST00000461690.5:c.67+180_67+181del	ENSP00000434298.1:n.67+180_67+181del
ENST00000466550.1:n.79+180_79+181del
ENST00000473558.5:n.303+180_303+181del
ENST00000483765.5:c.67+180_67+181del	ENSP00000473246.1:n.67+180_67+181del
ENST00000493317.1:c.67+180_67+181del	ENSP00000471695.1:n.67+180_67+181del
NM_000982.3:c.67+180_67+181del	NP_000973.2:n.67+180_67+181del
NM_000982.4:c.67+180_67+181del MANE Select	NP_000973.2:n.67+180_67+181del