Canonical Allele Identifier: CA954314936

Gene: RPL21

Linked Data

• dbSNP Id: rs1881765166
• gnomAD v3: 13-27253919-C-A
• gnomAD v4: 13-27253919-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27253919C>A , CM000675.2:g.27253919C>A	GRCh38
NC_000013.10:g.27828056C>A , CM000675.1:g.27828056C>A	GRCh37
NC_000013.9:g.26726056C>A	NCBI36
NG_046927.1:g.7365C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.67+76C>A MANE Select	ENSP00000346027.4:n.67+76C>A
ENST00000272274.8:c.67+76C>A	ENSP00000351021.2:n.67+76C>A
ENST00000311549.10:c.67+76C>A	ENSP00000346027.4:n.67+76C>A
ENST00000319826.8:c.67+76C>A	ENSP00000370574.1:n.67+76C>A
ENST00000326092.8:c.67+76C>A	ENSP00000370569.1:n.67+76C>A
ENST00000461690.5:c.67+76C>A	ENSP00000434298.1:n.67+76C>A
ENST00000466550.1:n.79+76C>A
ENST00000473558.5:n.303+76C>A
ENST00000483765.5:c.67+76C>A	ENSP00000473246.1:n.67+76C>A
ENST00000493317.1:c.67+76C>A	ENSP00000471695.1:n.67+76C>A
NM_000982.3:c.67+76C>A	NP_000973.2:n.67+76C>A
NM_000982.4:c.67+76C>A MANE Select	NP_000973.2:n.67+76C>A