Canonical Allele Identifier: CA2622452908

Gene: RPL21

Linked Data

• gnomAD v4: 13-27254068-CTGAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254071_27254074del , CM000675.2:g.27254071_27254074del	GRCh38
NC_000013.10:g.27828208_27828211del , CM000675.1:g.27828208_27828211del	GRCh37
NC_000013.9:g.26726208_26726211del	NCBI36
NG_046927.1:g.7517_7520del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.68-149_68-146del MANE Select	ENSP00000346027.4:n.68-149_68-146del
ENST00000272274.8:c.68-149_68-146del	ENSP00000351021.2:n.68-149_68-146del
ENST00000311549.10:c.68-149_68-146del	ENSP00000346027.4:n.68-149_68-146del
ENST00000319826.8:c.68-149_68-146del	ENSP00000370574.1:n.68-149_68-146del
ENST00000326092.8:c.68-149_68-146del	ENSP00000370569.1:n.68-149_68-146del
ENST00000461690.5:c.68-149_68-146del	ENSP00000434298.1:n.68-149_68-146del
ENST00000466550.1:n.80-149_80-146del
ENST00000473558.5:n.304-149_304-146del
ENST00000483765.5:c.67+228_67+231del	ENSP00000473246.1:n.67+228_67+231del
ENST00000493317.1:c.68-149_68-146del	ENSP00000471695.1:n.68-149_68-146del
NM_000982.3:c.68-149_68-146del	NP_000973.2:n.68-149_68-146del
NM_000982.4:c.68-149_68-146del MANE Select	NP_000973.2:n.68-149_68-146del