Canonical Allele Identifier: CA696955865

Gene: RPL21

Linked Data

• dbSNP Id: rs1475946419
• gnomAD v3: 13-27253998-TTA-T
• gnomAD v4: 13-27253998-TTA-T
• MyVariant Identifiers: chr13:g.27828136_27828137del (hg19) ; chr13:g.27253999_27254000del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254002_27254003del , CM000675.2:g.27254002_27254003del	GRCh38
NC_000013.10:g.27828139_27828140del , CM000675.1:g.27828139_27828140del	GRCh37
NC_000013.9:g.26726139_26726140del	NCBI36
NG_046927.1:g.7448_7449del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.67+159_67+160del MANE Select	ENSP00000346027.4:n.67+159_67+160del
ENST00000272274.8:c.67+159_67+160del	ENSP00000351021.2:n.67+159_67+160del
ENST00000311549.10:c.67+159_67+160del	ENSP00000346027.4:n.67+159_67+160del
ENST00000319826.8:c.67+159_67+160del	ENSP00000370574.1:n.67+159_67+160del
ENST00000326092.8:c.67+159_67+160del	ENSP00000370569.1:n.67+159_67+160del
ENST00000461690.5:c.67+159_67+160del	ENSP00000434298.1:n.67+159_67+160del
ENST00000466550.1:n.79+159_79+160del
ENST00000473558.5:n.303+159_303+160del
ENST00000483765.5:c.67+159_67+160del	ENSP00000473246.1:n.67+159_67+160del
ENST00000493317.1:c.67+159_67+160del	ENSP00000471695.1:n.67+159_67+160del
NM_000982.3:c.67+159_67+160del	NP_000973.2:n.67+159_67+160del
NM_000982.4:c.67+159_67+160del MANE Select	NP_000973.2:n.67+159_67+160del