Canonical Allele Identifier: CA2080454216

Gene: RPL21

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254131_27254133delinsGAT , CM000675.2:g.27254131_27254133delinsGAT	GRCh38
NC_000013.10:g.27828268_27828270delinsGAT , CM000675.1:g.27828268_27828270delinsGAT	GRCh37
NC_000013.9:g.26726268_26726270delinsGAT	NCBI36
NG_046927.1:g.7577_7579delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.68-89_68-87delinsGAT MANE Select	ENSP00000346027.4:n.68-89_68-87delinsGAT
ENST00000272274.8:c.68-89_68-87delinsGAT	ENSP00000351021.2:n.68-89_68-87delinsGAT
ENST00000311549.10:c.68-89_68-87delinsGAT	ENSP00000346027.4:n.68-89_68-87delinsGAT
ENST00000319826.8:c.68-89_68-87delinsGAT	ENSP00000370574.1:n.68-89_68-87delinsGAT
ENST00000326092.8:c.68-89_68-87delinsGAT	ENSP00000370569.1:n.68-89_68-87delinsGAT
ENST00000461690.5:c.68-89_68-87delinsGAT	ENSP00000434298.1:n.68-89_68-87delinsGAT
ENST00000466550.1:n.80-89_80-87delinsGAT
ENST00000473558.5:n.304-89_304-87delinsGAT
ENST00000483765.5:c.67+288_67+290delinsGAT	ENSP00000473246.1:n.67+288_67+290delinsGAT
ENST00000493317.1:c.68-89_68-87delinsGAT	ENSP00000471695.1:n.68-89_68-87delinsGAT
NM_000982.3:c.68-89_68-87delinsGAT	NP_000973.2:n.68-89_68-87delinsGAT
NM_000982.4:c.68-89_68-87delinsGAT MANE Select	NP_000973.2:n.68-89_68-87delinsGAT