Canonical Allele Identifier: CA2648114089

Gene: RPS27

Linked Data

• gnomAD v4: 1-153991233-C-CGTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991234_153991235insTCTG , CM000663.2:g.153991234_153991235insTCTG	GRCh38
NC_000001.10:g.153963710_153963711insTCTG , CM000663.1:g.153963710_153963711insTCTG	GRCh37
NC_000001.9:g.152230334_152230335insTCTG	NCBI36
NG_053102.2:g.5480_5481insTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.303+11_303+12insTCTG
ENST00000643794.1:c.236+11_236+12insTCTG	ENSP00000495765.1:n.236+11_236+12insTCTG
ENST00000651669.1:c.115+11_115+12insTCTG MANE Select	ENSP00000499044.1:n.115+11_115+12insTCTG
ENST00000368567.4:c.115+11_115+12insTCTG	ENSP00000357555.4:n.115+11_115+12insTCTG
ENST00000392558.4:c.126_127insTCTG	ENSP00000376341.4:p.Ala43SerfsTer5
ENST00000477151.1:n.270+11_270+12insTCTG
ENST00000493224.5:n.381+11_381+12insTCTG
NM_001030.4:c.115+11_115+12insTCTG	NP_001021.1:n.115+11_115+12insTCTG
NM_001030.6:c.115+11_115+12insTCTG MANE Select	NP_001021.1:n.115+11_115+12insTCTG
NM_001349946.1:c.19+11_19+12insTCTG	NP_001336875.1:n.19+11_19+12insTCTG
NM_001349947.1:c.19+11_19+12insTCTG	NP_001336876.1:n.19+11_19+12insTCTG
NM_001349946.2:c.19+11_19+12insTCTG	NP_001336875.1:n.19+11_19+12insTCTG
NM_001349947.2:c.19+11_19+12insTCTG	NP_001336876.1:n.19+11_19+12insTCTG