Canonical Allele Identifier: CA2480680477

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153991289T= , CM000663.2:g.153991289T=	GRCh38
NC_000001.10:g.153963765T= , CM000663.1:g.153963765T=	GRCh37
NC_000001.9:g.152230389T=	NCBI36
NG_053102.2:g.5535T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477151.2:n.303+66T=
ENST00000643794.1:c.236+66T=	ENSP00000495765.1:n.236+66T=
ENST00000651669.1:c.115+66T= MANE Select	ENSP00000499044.1:n.115+66T=
ENST00000368567.4:c.115+66T=	ENSP00000357555.4:n.115+66T=
ENST00000392558.4:c.181T=	ENSP00000376341.4:p.Leu61=
ENST00000477151.1:n.270+66T=
ENST00000493224.5:n.381+66T=
NM_001030.4:c.115+66T=	NP_001021.1:n.115+66T=
NM_001030.6:c.115+66T= MANE Select	NP_001021.1:n.115+66T=
NM_001349946.1:c.19+66T=	NP_001336875.1:n.19+66T=
NM_001349947.1:c.19+66T=	NP_001336876.1:n.19+66T=
NM_001349946.2:c.19+66T=	NP_001336875.1:n.19+66T=
NM_001349947.2:c.19+66T=	NP_001336876.1:n.19+66T=