Canonical Allele Identifier: CA696955834

Gene: RPL21

Linked Data

• dbSNP Id: rs1408177401
• gnomAD v3: 13-27253960-C-T
• gnomAD v4: 13-27253960-C-T
• MyVariant Identifiers: chr13:g.27828097C>T (hg19) ; chr13:g.27253960C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27253960C>T , CM000675.2:g.27253960C>T	GRCh38
NC_000013.10:g.27828097C>T , CM000675.1:g.27828097C>T	GRCh37
NC_000013.9:g.26726097C>T	NCBI36
NG_046927.1:g.7406C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.67+117C>T MANE Select	ENSP00000346027.4:n.67+117C>T
ENST00000272274.8:c.67+117C>T	ENSP00000351021.2:n.67+117C>T
ENST00000311549.10:c.67+117C>T	ENSP00000346027.4:n.67+117C>T
ENST00000319826.8:c.67+117C>T	ENSP00000370574.1:n.67+117C>T
ENST00000326092.8:c.67+117C>T	ENSP00000370569.1:n.67+117C>T
ENST00000461690.5:c.67+117C>T	ENSP00000434298.1:n.67+117C>T
ENST00000466550.1:n.79+117C>T
ENST00000473558.5:n.303+117C>T
ENST00000483765.5:c.67+117C>T	ENSP00000473246.1:n.67+117C>T
ENST00000493317.1:c.67+117C>T	ENSP00000471695.1:n.67+117C>T
NM_000982.3:c.67+117C>T	NP_000973.2:n.67+117C>T
NM_000982.4:c.67+117C>T MANE Select	NP_000973.2:n.67+117C>T