Canonical Allele Identifier: CA1148872078

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991130C= , CM000663.2:g.153991130C=	GRCh38
NC_000001.10:g.153963606C= , CM000663.1:g.153963606C=	GRCh37
NC_000001.9:g.152230230C=	NCBI36
NG_053102.2:g.5376C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.210C=
ENST00000643794.1:c.143C=	ENSP00000495765.1:p.Pro48=
ENST00000651669.1:c.22C= MANE Select	ENSP00000499044.1:p.Leu8=
ENST00000368567.4:c.22C=	ENSP00000357555.4:p.Leu8=
ENST00000392558.4:c.22C=	ENSP00000376341.4:p.Leu8=
ENST00000477151.1:n.177C=
ENST00000493224.5:n.288C=
NM_001030.4:c.22C=	NP_001021.1:p.Leu8=
NM_001030.6:c.22C= MANE Select	NP_001021.1:p.Leu8=
NM_001349946.1:c.-75C=	NP_001336875.1:n.-75C=
NM_001349947.1:c.-75C=	NP_001336876.1:n.-75C=
NM_001349946.2:c.-75C=	NP_001336875.1:n.-75C=
NM_001349947.2:c.-75C=	NP_001336876.1:n.-75C=