Canonical Allele Identifier: CA2480680316

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990927G= , CM000663.2:g.153990927G=	GRCh38
NC_000001.10:g.153963403G= , CM000663.1:g.153963403G=	GRCh37
NC_000001.9:g.152230027G=	NCBI36
NG_053102.2:g.5173G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.7G=
ENST00000643794.1:c.20G=	ENSP00000495765.1:p.Arg7=
ENST00000651669.1:c.6+125G= MANE Select	ENSP00000499044.1:n.6+125G=
ENST00000368567.4:c.6+125G=	ENSP00000357555.4:n.6+125G=
ENST00000392558.4:c.6+125G=	ENSP00000376341.4:n.6+125G=
ENST00000477151.1:n.54G=
ENST00000493224.5:n.165G=
NM_001030.4:c.6+125G=	NP_001021.1:n.6+125G=
NM_001030.6:c.6+125G= MANE Select	NP_001021.1:n.6+125G=
NM_001349946.1:c.-198G=	NP_001336875.1:n.-198G=
NM_001349947.1:c.-198G=	NP_001336876.1:n.-198G=
NM_001349946.2:c.-198G=	NP_001336875.1:n.-198G=
NM_001349947.2:c.-198G=	NP_001336876.1:n.-198G=