Canonical Allele Identifier: CA608718368

Gene: RPL21

Linked Data

• dbSNP Id: rs1487584759
• gnomAD v2: 13-27828085-ACTAGCGTCTAC-A
• gnomAD v3: 13-27253948-ACTAGCGTCTAC-A
• gnomAD v4: 13-27253948-ACTAGCGTCTAC-A
• MyVariant Identifiers: chr13:g.27828086_27828096del (hg19) ; chr13:g.27253949_27253959del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.27253950_27253960del , CM000675.2:g.27253950_27253960del	GRCh38
NC_000013.10:g.27828087_27828097del , CM000675.1:g.27828087_27828097del	GRCh37
NC_000013.9:g.26726087_26726097del	NCBI36
NG_046927.1:g.7396_7406del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311549.11:c.67+107_67+117del MANE Select	ENSP00000346027.4:n.67+107_67+117del
ENST00000272274.8:c.67+107_67+117del	ENSP00000351021.2:n.67+107_67+117del
ENST00000311549.10:c.67+107_67+117del	ENSP00000346027.4:n.67+107_67+117del
ENST00000319826.8:c.67+107_67+117del	ENSP00000370574.1:n.67+107_67+117del
ENST00000326092.8:c.67+107_67+117del	ENSP00000370569.1:n.67+107_67+117del
ENST00000461690.5:c.67+107_67+117del	ENSP00000434298.1:n.67+107_67+117del
ENST00000466550.1:n.79+107_79+117del
ENST00000473558.5:n.303+107_303+117del
ENST00000483765.5:c.67+107_67+117del	ENSP00000473246.1:n.67+107_67+117del
ENST00000493317.1:c.67+107_67+117del	ENSP00000471695.1:n.67+107_67+117del
NM_000982.3:c.67+107_67+117del	NP_000973.2:n.67+107_67+117del
NM_000982.4:c.67+107_67+117del MANE Select	NP_000973.2:n.67+107_67+117del