Canonical Allele Identifier: CA2480680422

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991148G= , CM000663.2:g.153991148G=	GRCh38
NC_000001.10:g.153963624G= , CM000663.1:g.153963624G=	GRCh37
NC_000001.9:g.152230248G=	NCBI36
NG_053102.2:g.5394G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.228G=
ENST00000643794.1:c.161G=	ENSP00000495765.1:p.Arg54=
ENST00000651669.1:c.40G= MANE Select	ENSP00000499044.1:p.Glu14=
ENST00000368567.4:c.40G=	ENSP00000357555.4:p.Glu14=
ENST00000392558.4:c.40G=	ENSP00000376341.4:p.Glu14=
ENST00000477151.1:n.195G=
ENST00000493224.5:n.306G=
NM_001030.4:c.40G=	NP_001021.1:p.Glu14=
NM_001030.6:c.40G= MANE Select	NP_001021.1:p.Glu14=
NM_001349946.1:c.-57G=	NP_001336875.1:n.-57G=
NM_001349947.1:c.-57G=	NP_001336876.1:n.-57G=
NM_001349946.2:c.-57G=	NP_001336875.1:n.-57G=
NM_001349947.2:c.-57G=	NP_001336876.1:n.-57G=