Canonical Allele Identifier: CA387623105

Gene: RPL21

Linked Data

• gnomAD v4: 13-27254237-A-C
• MyVariant Identifiers: chr13:g.27828374A>C (hg19) ; chr13:g.27254237A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27254237A>C , CM000675.2:g.27254237A>C	GRCh38
NC_000013.10:g.27828374A>C , CM000675.1:g.27828374A>C	GRCh37
NC_000013.9:g.26726374A>C	NCBI36
NG_046927.1:g.7683A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.85A>C MANE Select	ENSP00000346027.4:p.Thr29Pro
ENST00000272274.8:c.85A>C	ENSP00000351021.2:p.Thr29Pro
ENST00000311549.10:c.85A>C	ENSP00000346027.4:p.Thr29Pro
ENST00000319826.8:c.85A>C	ENSP00000370574.1:p.Thr29Pro
ENST00000326092.8:c.85A>C	ENSP00000370569.1:p.Thr29Pro
ENST00000461690.5:c.85A>C	ENSP00000434298.1:p.Thr29Pro
ENST00000466550.1:n.97A>C
ENST00000473558.5:n.321A>C
ENST00000483765.5:c.67+394A>C	ENSP00000473246.1:n.67+394A>C
ENST00000493317.1:c.85A>C	ENSP00000471695.1:p.Thr29Pro
NM_000982.3:c.85A>C	NP_000973.2:p.Thr29Pro
NM_000982.4:c.85A>C MANE Select	NP_000973.2:p.Thr29Pro