Canonical Allele Identifier: CA2480680409

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991123G= , CM000663.2:g.153991123G=	GRCh38
NC_000001.10:g.153963599G= , CM000663.1:g.153963599G=	GRCh37
NC_000001.9:g.152230223G=	NCBI36
NG_053102.2:g.5369G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.203G=
ENST00000643794.1:c.136G=	ENSP00000495765.1:p.Gly46=
ENST00000651669.1:c.15G= MANE Select	ENSP00000499044.1:p.Lys5=
ENST00000368567.4:c.15G=	ENSP00000357555.4:p.Lys5=
ENST00000392558.4:c.15G=	ENSP00000376341.4:p.Lys5=
ENST00000477151.1:n.170G=
ENST00000493224.5:n.281G=
NM_001030.4:c.15G=	NP_001021.1:p.Lys5=
NM_001030.6:c.15G= MANE Select	NP_001021.1:p.Lys5=
NM_001349946.1:c.-82G=	NP_001336875.1:n.-82G=
NM_001349947.1:c.-82G=	NP_001336876.1:n.-82G=
NM_001349946.2:c.-82G=	NP_001336875.1:n.-82G=
NM_001349947.2:c.-82G=	NP_001336876.1:n.-82G=