Canonical Allele Identifier: CA1141746911

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990782T= , CM000663.2:g.153990782T=	GRCh38
NC_000001.10:g.153963258T= , CM000663.1:g.153963258T=	GRCh37
NC_000001.9:g.152229882T=	NCBI36
NG_053102.2:g.5028T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.-15T=	ENSP00000495765.1:n.-15T=
ENST00000651669.1:c.-15T= MANE Select	ENSP00000499044.1:n.-15T=
ENST00000368567.4:c.-15T=	ENSP00000357555.4:n.-15T=
ENST00000392558.4:c.-15T=	ENSP00000376341.4:n.-15T=
ENST00000477151.1:n.20T=
ENST00000493224.5:n.20T=
NM_001030.4:c.-15T=	NP_001021.1:n.-15T=
NM_001030.6:c.-15T= MANE Select	NP_001021.1:n.-15T=
NM_001349946.1:c.-232T=	NP_001336875.1:n.-232T=
NM_001349947.1:c.-343T=	NP_001336876.1:n.-343T=
NM_001349946.2:c.-232T=	NP_001336875.1:n.-232T=
NM_001349947.2:c.-343T=	NP_001336876.1:n.-343T=