Canonical Allele Identifier: CA1146902751

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990780C= , CM000663.2:g.153990780C=	GRCh38
NC_000001.10:g.153963256C= , CM000663.1:g.153963256C=	GRCh37
NC_000001.9:g.152229880C=	NCBI36
NG_053102.2:g.5026C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.-17C=	ENSP00000495765.1:n.-17C=
ENST00000651669.1:c.-17C= MANE Select	ENSP00000499044.1:n.-17C=
ENST00000368567.4:c.-17C=	ENSP00000357555.4:n.-17C=
ENST00000392558.4:c.-17C=	ENSP00000376341.4:n.-17C=
ENST00000477151.1:n.18C=
ENST00000493224.5:n.18C=
NM_001030.4:c.-17C=	NP_001021.1:n.-17C=
NM_001030.6:c.-17C= MANE Select	NP_001021.1:n.-17C=
NM_001349946.1:c.-234C=	NP_001336875.1:n.-234C=
NM_001349947.1:c.-345C=	NP_001336876.1:n.-345C=
NM_001349946.2:c.-234C=	NP_001336875.1:n.-234C=
NM_001349947.2:c.-345C=	NP_001336876.1:n.-345C=