Canonical Allele Identifier: CA2480680441

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991225_153991228delinsTGAG , CM000663.2:g.153991225_153991228delinsTGAG	GRCh38
NC_000001.10:g.153963701_153963704delinsTGAG , CM000663.1:g.153963701_153963704delinsTGAG	GRCh37
NC_000001.9:g.152230325_152230328delinsTGAG	NCBI36
NG_053102.2:g.5471_5474delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.303+2_303+5delinsTGAG
ENST00000643794.1:c.236+2_236+5delinsTGAG	ENSP00000495765.1:n.236+2_236+5delinsTGAG
ENST00000651669.1:c.115+2_115+5delinsTGAG MANE Select	ENSP00000499044.1:n.115+2_115+5delinsTGAG
ENST00000368567.4:c.115+2_115+5delinsTGAG	ENSP00000357555.4:n.115+2_115+5delinsTGAG
ENST00000392558.4:c.117_120delinsTGAG	ENSP00000376341.4:p.Gly39=
ENST00000477151.1:n.270+2_270+5delinsTGAG
ENST00000493224.5:n.381+2_381+5delinsTGAG
NM_001030.4:c.115+2_115+5delinsTGAG	NP_001021.1:n.115+2_115+5delinsTGAG
NM_001030.6:c.115+2_115+5delinsTGAG MANE Select	NP_001021.1:n.115+2_115+5delinsTGAG
NM_001349946.1:c.19+2_19+5delinsTGAG	NP_001336875.1:n.19+2_19+5delinsTGAG
NM_001349947.1:c.19+2_19+5delinsTGAG	NP_001336876.1:n.19+2_19+5delinsTGAG
NM_001349946.2:c.19+2_19+5delinsTGAG	NP_001336875.1:n.19+2_19+5delinsTGAG
NM_001349947.2:c.19+2_19+5delinsTGAG	NP_001336876.1:n.19+2_19+5delinsTGAG