Canonical Allele Identifier: CA696955858

Gene: RPL21

Linked Data

• dbSNP Id: rs1410890204
• gnomAD v4: 13-27253980-GTAAA-G
• MyVariant Identifiers: chr13:g.27828118_27828121del (hg19) ; chr13:g.27253981_27253984del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27253986_27253989del , CM000675.2:g.27253986_27253989del	GRCh38
NC_000013.10:g.27828123_27828126del , CM000675.1:g.27828123_27828126del	GRCh37
NC_000013.9:g.26726123_26726126del	NCBI36
NG_046927.1:g.7432_7435del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.67+143_67+146del MANE Select	ENSP00000346027.4:n.67+143_67+146del
ENST00000272274.8:c.67+143_67+146del	ENSP00000351021.2:n.67+143_67+146del
ENST00000311549.10:c.67+143_67+146del	ENSP00000346027.4:n.67+143_67+146del
ENST00000319826.8:c.67+143_67+146del	ENSP00000370574.1:n.67+143_67+146del
ENST00000326092.8:c.67+143_67+146del	ENSP00000370569.1:n.67+143_67+146del
ENST00000461690.5:c.67+143_67+146del	ENSP00000434298.1:n.67+143_67+146del
ENST00000466550.1:n.79+143_79+146del
ENST00000473558.5:n.303+143_303+146del
ENST00000483765.5:c.67+143_67+146del	ENSP00000473246.1:n.67+143_67+146del
ENST00000493317.1:c.67+143_67+146del	ENSP00000471695.1:n.67+143_67+146del
NM_000982.3:c.67+143_67+146del	NP_000973.2:n.67+143_67+146del
NM_000982.4:c.67+143_67+146del MANE Select	NP_000973.2:n.67+143_67+146del