Canonical Allele Identifier: CA483010064

Gene: RPL21

Linked Data

• MyVariant Identifiers: chr13:g.27828385A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254248A>T , CM000675.2:g.27254248A>T	GRCh38
NC_000013.10:g.27828385A>T , CM000675.1:g.27828385A>T	GRCh37
NC_000013.9:g.26726385A>T	NCBI36
NG_046927.1:g.7694A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.96A>T MANE Select	ENSP00000346027.4:p.Arg32=
ENST00000272274.8:c.96A>T	ENSP00000351021.2:p.Arg32=
ENST00000311549.10:c.96A>T	ENSP00000346027.4:p.Arg32=
ENST00000319826.8:c.96A>T	ENSP00000370574.1:p.Arg32=
ENST00000326092.8:c.96A>T	ENSP00000370569.1:p.Arg32=
ENST00000461690.5:c.96A>T	ENSP00000434298.1:p.Arg32=
ENST00000466550.1:n.108A>T
ENST00000473558.5:n.332A>T
ENST00000483765.5:c.67+405A>T	ENSP00000473246.1:n.67+405A>T
ENST00000493317.1:c.96A>T	ENSP00000471695.1:p.Arg32=
NM_000982.3:c.96A>T	NP_000973.2:p.Arg32=
NM_000982.4:c.96A>T MANE Select	NP_000973.2:p.Arg32=