Canonical Allele Identifier: CA2559823104
Gene: RPL21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.27253994_27253995insTGTTTTCTAAAAGGCCTAG , CM000675.2:g.27253994_27253995insTGTTTTCTAAAAGGCCTAG GRCh38
NC_000013.10:g.27828131_27828132insTGTTTTCTAAAAGGCCTAG , CM000675.1:g.27828131_27828132insTGTTTTCTAAAAGGCCTAG GRCh37
NC_000013.9:g.26726131_26726132insTGTTTTCTAAAAGGCCTAG NCBI36
NG_046927.1:g.7440_7441insTGTTTTCTAAAAGGCCTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000311549.11:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG MANE Select ENSP00000346027.4:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
ENST00000272274.8:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG ENSP00000351021.2:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
ENST00000311549.10:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG ENSP00000346027.4:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
ENST00000319826.8:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG ENSP00000370574.1:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
ENST00000326092.8:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG ENSP00000370569.1:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
ENST00000461690.5:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG ENSP00000434298.1:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
ENST00000466550.1:n.79+151_79+152insTGTTTTCTAAAAGGCCTAG
ENST00000473558.5:n.303+151_303+152insTGTTTTCTAAAAGGCCTAG
ENST00000483765.5:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG ENSP00000473246.1:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
ENST00000493317.1:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG ENSP00000471695.1:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
NM_000982.3:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG NP_000973.2:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG
NM_000982.4:c.67+151_67+152insTGTTTTCTAAAAGGCCTAG MANE Select NP_000973.2:n.67+151_67+152insTGTTTTCTAAAAGGCCTAG