Canonical Allele Identifier: CA2648113993

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991004-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991006del , CM000663.2:g.153991006del	GRCh38
NC_000001.10:g.153963482del , CM000663.1:g.153963482del	GRCh37
NC_000001.9:g.152230106del	NCBI36
NG_053102.2:g.5252del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.86del
ENST00000643794.1:c.99del	ENSP00000495765.1:p.Arg34GlyfsTer?
ENST00000651669.1:c.7-109del MANE Select	ENSP00000499044.1:n.7-109del
ENST00000368567.4:c.7-109del	ENSP00000357555.4:n.7-109del
ENST00000392558.4:c.7-109del	ENSP00000376341.4:n.7-109del
ENST00000477151.1:n.133del
ENST00000493224.5:n.244del
NM_001030.4:c.7-109del	NP_001021.1:n.7-109del
NM_001030.6:c.7-109del MANE Select	NP_001021.1:n.7-109del
NM_001349946.1:c.-119del	NP_001336875.1:n.-119del
NM_001349947.1:c.-119del	NP_001336876.1:n.-119del
NM_001349946.2:c.-119del	NP_001336875.1:n.-119del
NM_001349947.2:c.-119del	NP_001336876.1:n.-119del