Canonical Allele Identifier: CA1141487117

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990787A= , CM000663.2:g.153990787A=	GRCh38
NC_000001.10:g.153963263A= , CM000663.1:g.153963263A=	GRCh37
NC_000001.9:g.152229887A=	NCBI36
NG_053102.2:g.5033A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.-10A=	ENSP00000495765.1:n.-10A=
ENST00000651669.1:c.-10A= MANE Select	ENSP00000499044.1:n.-10A=
ENST00000368567.4:c.-10A=	ENSP00000357555.4:n.-10A=
ENST00000392558.4:c.-10A=	ENSP00000376341.4:n.-10A=
ENST00000477151.1:n.25A=
ENST00000493224.5:n.25A=
NM_001030.4:c.-10A=	NP_001021.1:n.-10A=
NM_001030.6:c.-10A= MANE Select	NP_001021.1:n.-10A=
NM_001349946.1:c.-227A=	NP_001336875.1:n.-227A=
NM_001349947.1:c.-338A=	NP_001336876.1:n.-338A=
NM_001349946.2:c.-227A=	NP_001336875.1:n.-227A=
NM_001349947.2:c.-338A=	NP_001336876.1:n.-338A=