Canonical Allele Identifier: CA2648114099

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991303-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991305del , CM000663.2:g.153991305del	GRCh38
NC_000001.10:g.153963781del , CM000663.1:g.153963781del	GRCh37
NC_000001.9:g.152230405del	NCBI36
NG_053102.2:g.5551del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.303+82del
ENST00000643794.1:c.236+82del	ENSP00000495765.1:n.236+82del
ENST00000651669.1:c.115+82del MANE Select	ENSP00000499044.1:n.115+82del
ENST00000368567.4:c.115+82del	ENSP00000357555.4:n.115+82del
ENST00000392558.4:c.197del	ENSP00000376341.4:p.Pro66LeufsTer?
ENST00000477151.1:n.270+82del
ENST00000493224.5:n.381+82del
NM_001030.4:c.115+82del	NP_001021.1:n.115+82del
NM_001030.6:c.115+82del MANE Select	NP_001021.1:n.115+82del
NM_001349946.1:c.19+82del	NP_001336875.1:n.19+82del
NM_001349947.1:c.19+82del	NP_001336876.1:n.19+82del
NM_001349946.2:c.19+82del	NP_001336875.1:n.19+82del
NM_001349947.2:c.19+82del	NP_001336876.1:n.19+82del