Canonical Allele Identifier: CA2080454296

Gene: RPL21

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254334_27254336delinsAAT , CM000675.2:g.27254334_27254336delinsAAT	GRCh38
NC_000013.10:g.27828471_27828473delinsAAT , CM000675.1:g.27828471_27828473delinsAAT	GRCh37
NC_000013.9:g.26726471_26726473delinsAAT	NCBI36
NG_046927.1:g.7780_7782delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.129+53_129+55delinsAAT MANE Select	ENSP00000346027.4:n.129+53_129+55delinsAAT
ENST00000272274.8:c.129+53_129+55delinsAAT	ENSP00000351021.2:n.129+53_129+55delinsAAT
ENST00000311549.10:c.129+53_129+55delinsAAT	ENSP00000346027.4:n.129+53_129+55delinsAAT
ENST00000319826.8:c.129+53_129+55delinsAAT	ENSP00000370574.1:n.129+53_129+55delinsAAT
ENST00000326092.8:c.129+53_129+55delinsAAT	ENSP00000370569.1:n.129+53_129+55delinsAAT
ENST00000461690.5:c.129+53_129+55delinsAAT	ENSP00000434298.1:n.129+53_129+55delinsAAT
ENST00000466550.1:n.141+53_141+55delinsAAT
ENST00000473558.5:n.418_420delinsAAT
ENST00000483765.5:c.67+491_67+493delinsAAT	ENSP00000473246.1:n.67+491_67+493delinsAAT
ENST00000493317.1:c.129+53_129+55delinsAAT	ENSP00000471695.1:n.129+53_129+55delinsAAT
NM_000982.3:c.129+53_129+55delinsAAT	NP_000973.2:n.129+53_129+55delinsAAT
NM_000982.4:c.129+53_129+55delinsAAT MANE Select	NP_000973.2:n.129+53_129+55delinsAAT