Canonical Allele Identifier: CA1144023362

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990786C= , CM000663.2:g.153990786C=	GRCh38
NC_000001.10:g.153963262C= , CM000663.1:g.153963262C=	GRCh37
NC_000001.9:g.152229886C=	NCBI36
NG_053102.2:g.5032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.-11C=	ENSP00000495765.1:n.-11C=
ENST00000651669.1:c.-11C= MANE Select	ENSP00000499044.1:n.-11C=
ENST00000368567.4:c.-11C=	ENSP00000357555.4:n.-11C=
ENST00000392558.4:c.-11C=	ENSP00000376341.4:n.-11C=
ENST00000477151.1:n.24C=
ENST00000493224.5:n.24C=
NM_001030.4:c.-11C=	NP_001021.1:n.-11C=
NM_001030.6:c.-11C= MANE Select	NP_001021.1:n.-11C=
NM_001349946.1:c.-228C=	NP_001336875.1:n.-228C=
NM_001349947.1:c.-339C=	NP_001336876.1:n.-339C=
NM_001349946.2:c.-228C=	NP_001336875.1:n.-228C=
NM_001349947.2:c.-339C=	NP_001336876.1:n.-339C=