Canonical Allele Identifier: CA1148562291

Gene: RPS27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153990781C= , CM000663.2:g.153990781C=	GRCh38
NC_000001.10:g.153963257C= , CM000663.1:g.153963257C=	GRCh37
NC_000001.9:g.152229881C=	NCBI36
NG_053102.2:g.5027C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643794.1:c.-16C=	ENSP00000495765.1:n.-16C=
ENST00000651669.1:c.-16C= MANE Select	ENSP00000499044.1:n.-16C=
ENST00000368567.4:c.-16C=	ENSP00000357555.4:n.-16C=
ENST00000392558.4:c.-16C=	ENSP00000376341.4:n.-16C=
ENST00000477151.1:n.19C=
ENST00000493224.5:n.19C=
NM_001030.4:c.-16C=	NP_001021.1:n.-16C=
NM_001030.6:c.-16C= MANE Select	NP_001021.1:n.-16C=
NM_001349946.1:c.-233C=	NP_001336875.1:n.-233C=
NM_001349947.1:c.-344C=	NP_001336876.1:n.-344C=
NM_001349946.2:c.-233C=	NP_001336875.1:n.-233C=
NM_001349947.2:c.-344C=	NP_001336876.1:n.-344C=