Canonical Allele Identifier: CA2080454161

Gene: RPL21

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27253998_27254000delinsTTA , CM000675.2:g.27253998_27254000delinsTTA	GRCh38
NC_000013.10:g.27828135_27828137delinsTTA , CM000675.1:g.27828135_27828137delinsTTA	GRCh37
NC_000013.9:g.26726135_26726137delinsTTA	NCBI36
NG_046927.1:g.7444_7446delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.67+155_67+157delinsTTA MANE Select	ENSP00000346027.4:n.67+155_67+157delinsTTA
ENST00000272274.8:c.67+155_67+157delinsTTA	ENSP00000351021.2:n.67+155_67+157delinsTTA
ENST00000311549.10:c.67+155_67+157delinsTTA	ENSP00000346027.4:n.67+155_67+157delinsTTA
ENST00000319826.8:c.67+155_67+157delinsTTA	ENSP00000370574.1:n.67+155_67+157delinsTTA
ENST00000326092.8:c.67+155_67+157delinsTTA	ENSP00000370569.1:n.67+155_67+157delinsTTA
ENST00000461690.5:c.67+155_67+157delinsTTA	ENSP00000434298.1:n.67+155_67+157delinsTTA
ENST00000466550.1:n.79+155_79+157delinsTTA
ENST00000473558.5:n.303+155_303+157delinsTTA
ENST00000483765.5:c.67+155_67+157delinsTTA	ENSP00000473246.1:n.67+155_67+157delinsTTA
ENST00000493317.1:c.67+155_67+157delinsTTA	ENSP00000471695.1:n.67+155_67+157delinsTTA
NM_000982.3:c.67+155_67+157delinsTTA	NP_000973.2:n.67+155_67+157delinsTTA
NM_000982.4:c.67+155_67+157delinsTTA MANE Select	NP_000973.2:n.67+155_67+157delinsTTA